JP3606618B2 - Method for producing high purity optically active alcohol - Google Patents

Description

一般式（１）
〔但し、式（１）中、Ａ≠Ｂであり、Ａはフェニル基または下記一般式（２）
【化６】

一般式（２）
（式（２）においてＤ_１、Ｄ_２、Ｄ_３、Ｄ_４およびＤ_５はハロゲン原子、炭素数１〜３のアルキル基または炭素数１〜３のアルコキシ基）で表される置換基であり、Ｂは炭素数１〜３のアルキル基またはＣＦ_３またはＣＮ〕で表されるラセミ体アルコールであれば、以下に述べる本発明の方法により効率良く光学分割を行うことができる。
【０００９】
具体的には２−ブタノール、２−ペンタノール、２−ヘキサノール、２−ヘプタノール、２−オクタノール、２−ノナノール、２−デカノール、１−フェニルエタノール、１−フェニル−１−プロパノール、エチル−３−ヒドロキシ−ブタネート、エチル−３−ヒドロキシ−プロピオネート、メチル−３−ヒドロキシ−ペンタネート、１−フェニル−１，３−プロパンジオール、２−フェニル−１−シクロヘキサノール、１−ペンチン−３−オール、１−（２−ブロモフェニル）エタノール、１−パラクロロフェニルエタノール、１−（４−クロロフェニル）エタノール、１−クロロ−２−オクタノール、１，１−ジフルオロ−２−オクタノール、１−（２，４−ジクロロフェニル）エタノール等のラセミ体アルコールがある。このうち、好ましくは２−オクタノール、１−フェニルエタノール、１−フェニル−１，３−プロパンジオール、２−フェニル−１−シクロヘキサノールであり、最も好ましくは１−フェニルエタノール、２−オクタノール、１−（２−ブロモフェニル）エタノールである。
【００１０】
本発明に用いる１，３−プロパンジオールは、その２位炭素に同一あるいは異なる２種類のアルキル基が置換もしくは非置換したものであり、ここにアルキル基とはメチル基、エチル基、ｎ−プロピル基、イソプロピル基、ｎ−ブチル基およびｓｅｃ−ブチル基からなる群より選ばれるものであって、具体例として１，３−プロパンジオール、２，２−ジメチル−１，３−プロパンジオール（ネオペンチルグリコール）、２，２−ジエチル−１，３−プロパンジオール、２，２−ジｎ−プロピル−１，３−プロパンジオール、２，２−ジｎ−ブチル−１，３−プロパンジオール、２−メチル−２−エチル−１，３−プロパンジオール、２−メチル−２−ｎ−プロピル−１，３−プロパンジオール、２−メチル−２−ｎ−ブチル−１，３−プロパンジオール、２−エチル−２−ｎ−プロピル−１，３−プロパンジオール、２−エチル−２−ｎ−ブチル−１，３−プロパンジオール、２−ｎ−プロピル−２−ｎ−ブチル−１，３−プロパンジオール等をあげることができる。このうちアルキル基が非置換の１，３−プロパンジオール、さらには２，２−ジメチル−１，３−プロパンジオール、２，２−ジエチル−１，３−プロパンジオールがより好ましく、また１，３−プロパンジオールが最も好ましい。
【００１１】
本発明で用いるエステルとは前記１，３−プロパンジオールと炭素数が１６以上の脂肪酸とのエステルをいい、１，３−プロパンジオールのパルミチン酸エステル、２−ヘキシルデカン酸エステル、パルミトオレイン酸エステル、ステアリン酸エステル、イソステアリン酸（２−ヘプチルウンデカン酸、エメリー社製イソステアリン酸等）エステル、オレイン酸エステル、リノール酸エステル、リノレン酸エステル、アラキジン酸エステル、ベヘン酸エステル、エルシン酸エステル、リグノセリン酸エステル、セロチン酸エステル、モンタン酸エステル、メリシン酸エステル等を具体的に例示できる。これらのエステルは任意の割合の混合物としても使用でき、またその構成脂肪酸も植物油脂（大豆油、菜種油、オリーブ油、コーン油、サフラワー油、ひまわり油、綿実油、パーム油等）、動物油脂（牛脂、豚脂等）、魚油（イワシ油、サンマ油、タラ肝油等）を加水分解して得られる混合脂肪酸、それらの水素添加物を用いてもよい。このうち好ましいエステルは１，３−プロパンジオールのパルミチン酸エステル、ステアリン酸エステル、オレイン酸エステル、ベヘン酸エステル（いずれも直鎖状脂肪酸のエステル）であり、最も好ましくはステアリン酸エステル、ベヘン酸エステルである。また、モノエステルでもジエステルでも使用できるが、エステル交換反応の効率性の点からジエステルが望ましい。前記エステルは、望ましくは炭素数が１８以上３０程度までの直鎖状飽和脂肪酸で構成されるものであって、高融点（好ましくは６０℃以上、より好ましくは７０℃以上）であることを特徴とする。これにより、本発明のエステル交換反応物から目的の光学活性アルコールを効率良く分離できる利点がある。
【００１２】
なおラセミ体アルコールと反応させるエステルは１，３−プロパンジオールの脂肪酸エステルである必要があり、１価アルコールの脂肪酸エステルでは蒸留処理の際に不純物が混入し、高純度の光学活性アルコールが得られない。またトリグリセリドを用いるとエステル交換反応は進行するものの、リパーゼが１、３特異性である場合、生成した１，２型ジグリセリドが１，３型ジグリセリドに転移し、２段目反応で減圧操作を行っても光学活性アルコールが再び遊離することはない。さらには、４価以上の多価アルコールのエステルでは反応速度が極端に低下してしまう。
【００１３】
本発明のエステル交換反応では、耐熱性リパーゼを用いることを特徴とする。これによりエステル交換反応を高温に維持して速やかに進行させることができ、さらにまた高温かつ減圧下でエステル交換反応を行うことができ、該反応を進めながら反応生成物として発生してくる光学活性アルコールを同時に回収することが可能となる。
【００１４】
耐熱性リパーゼとしては、特公昭５８−３６９５３号公報に記載のアルカリゲネス（Ａｌｃａｌｉｇｅｎｅｓ ）属由来のリパーゼ、特開昭５９−１５６２８２号公報に記載のリゾプス キネンシス（Ｒｈｉｚｏｐｕｓ ｃｈｉｎｅｎｓｉｓ）等を例示できる。本発明ではとりわけ、特公昭５８−３６９５３号公報に記載されたアルカリゲネス エスピー（Ａｌｃａｌｉｇｅｎｅｓ ｓｐ．ＰＬ−２６６）（微工研菌寄第３１８７号）が生産するリパーゼＰＬ−２６６、特公昭６０−１５３１２号公報に記載のアルカリゲネス
エスピー（Ａｌｃａｌｉｇｅｎｅｓ ｓｐ． ＰＬ−６７９）（微工研菌寄第３７８３号）が生産するリパーゼＰＬ−６７９が好ましく、さらには名糖産業（株）製のリパーゼＱＬが望ましい。かかる耐熱性リパーゼは、活性炭、セライト、吸着性樹脂、イオン交換樹脂、セラミックス等の公知の担体に固定化してもよいが、後述するように粉末状態のままで原料に共存させることが望ましい。
【００１５】
エステル交換反応は、前記したラセミ体アルコールとエステルとをラセミ体アルコールを基準にして１：５以下、好ましくは１：２〜１のモル比率で原料として混合し、該原料の溶媒を使用することなく、なおかつ実質的に水分を含まない（すなわち原料中の平衡水分含量である約０．１重量％以下、望ましくは０．０５重量％以下の）反応系に、好ましくは前記リパーゼの粉末を分散させて、攪拌しながら反応を行う。このときリパーゼ粉末の粒子の９０％以上が１〜１００μｍ、好ましくは２０〜５０μｍの大きさになるようにコントロールしてエステル交換反応を行うことが望ましい。この粒子サイズをそろえる手段としては、必要に応じて加温し溶解した原料にリパーゼ粉末を分散させた後、超音波処理、分散液の精密膜または限外濾過膜による濾過処理、遠心沈降処理等を施せばよいが、好ましくは反応温度以下、２０〜１５０ｋＨｚ 、１００〜２５０Ｗの条件下で１〜３０分間超音波を照射処理することが簡便である。
【００１６】
反応温度は８１℃以上、より好ましくは９１〜１３０℃、最も好ましくは１０１〜１２０℃に設定し、エステル交換（本発明ではアルコリシス）反応を１回行う場合、および２回行う場合の１段目の該反応のときには、常圧状態で、緩やかに攪拌もしくは振とうしながら、反応率を例えばガスクロマトグラフィーでチェックして、所定の時間、望ましくは数時間から１００時間、エステル交換反応を行わせる。反応温度が８１℃を下回ると該反応の進行が遅く、逆に１３０℃を超えるとリパーゼの失活を招く。この反応によってラセミ体アルコールの鏡像異性体（Ｒ体またはＳ体）のいずれか一方が前記１，３−プロパンジオールの脂肪酸エステルとエステル交換（アルコリシス）され、Ｒ体またはＳ体のいずれか一方の光学活性アルコールの脂肪酸エステルと未反応の光学活性アルコールとを生じる。かかる成分を含むエステル交換反応物は、これから耐熱性リパーゼを濾別して除去しもしくは除去せずに減圧状態（５〜１ｍｍＨｇ）で前記未反応の光学活性アルコールを蒸留し、またエステル交換反応した光学活性アルコールの脂肪酸エステルを分別、再結晶、シリカゲルカラムクロマトグラフィー等の公知の方法で分離し、酸またはアルカリ加水分解して、他方の光学活性アルコールを得ることができる。本発明ではこれによりＲ体およびＳ体の各光学活性アルコールを高純度化できる。
【００１７】
なお、本発明では、以下に述べる実施態様がより好ましく、これによりラセミ体アルコールからＲ体およびＳ体の各光学活性アルコールの高純度品をさらに簡便に高収率で得ることが可能となる。すなわちラセミ体アルコールと、２位炭素にアルキル基が置換もしくは非置換の１，３−プロパンジオールの炭素数１６以上の脂肪酸エステルとを、まず前記と同様の条件すなわち耐熱性リパーゼの存在下、溶媒を用いることなく、かつ実質的に水分を含まない条件下で、８１℃以上にて常圧状態でエステル交換反応（１段目反応）を行い、該反応終了後、未反応のＲ体またはＳ体のいずれか一方に富む光学活性アルコールを減圧蒸留して分離する。これにより該蒸留処理した残分中には、エステル交換したＲ体またはＳ体のいずれか一方の光学活性アルコール（減圧蒸留されなかった鏡像異性体の他方）の脂肪酸エステル、原料として用いた前記１，３−プロパンジオールの脂肪酸エステルが部分的ないし完全に加アルコール分解された成分等が共存することになる。
【００１８】
１段目反応にひき続き２段目反応では前記残分をそのまま減圧状態（５〜１ｍｍＨｇ）に維持して、１段目反応と同様の条件下（耐熱性リパーゼの共存下、無溶媒かつ実質的無水の条件で８１℃以上）でエステル交換（アルコリシス）反応させ、該反応により生成してくるＲ体またはＳ体のいずれか一方の光学活性アルコールを、望ましくは該反応を行いながらあるいは該反応終了後に減圧蒸留して分離する。ここで耐熱性リパーゼは１段目反応に用いたものをそのまま反応物に共存させて２段目反応を行わせることが簡便であるが、２段目反応開始時に新たに添加してもよい。
かくしてラセミ体アルコールから高純度のＲ体およＳ体の各光学活性アルコールを容易に高収率で分割することができる。
【００１９】
【実施例】
以下の実施例および比較例において得られた化合物の物質純度はガスクロマトグラフィー（（株）島津製作所製、ＧＣ−１４Ａ）を用いて、また光学純度は比旋光度を旋光度計（日本分光（株）製、ＤＩＰ−３７０）を用いてそれぞれ測定し、その測定値を標準試料の値と比較することにより算出した。
【００２０】
実施例１
アルカリゲネス エスピー（Ａｌｃａｌｉｇｅｎｅｓ ｓｐ．）由来のリパーゼＱＬ （名糖産業（株）製）３ｇ、（Ｒ，Ｓ）−１−フェニルエタノール５０ｇおよび１，３−プロパンジオールのオレイン酸ジエステル（１，３−プロパンジオールとオレイン酸とを、パラトルエンスルホン酸を触媒とし、１５０〜２００℃で５時間エステル化反応させて得たもの。純度：９９％。）２７０ｇを５００ｍｌセパラブルフラスコに入れ、室温で超音波発生装置（（株）島津製作所製、ＳＵＳ−１０３）を用いて４５ｋＨｚ で１分間超音波を照射した。その後、９０℃にて攪拌速度３５０ｒｐｍ で攪拌し、常圧状態で２４時間エステル交換反応を行った。反応系の水分量（カールフィッシャー法）：０．０５重量％、リパーゼ粒子のサイズ（コールターエレクトロニクス社製の粒度分布測定装置：マルチサイザーによる測定）：９５％以上が２０〜５０μｍであった。反応終了後、反応物をガスクロマトグラフィーで測定したところ、（Ｒ，Ｓ）−１−フェニルエタノールの４９モル％がオレイン酸エステルに変換されていた。そのまま反応系内を９０℃、１ｍｍＨｇに減圧して２０分間蒸留し、未反応の（Ｓ）−（−）−１−フェニルエタノール（収率：９８％、物質純度：１００％、光学純度：９９％ｅｅ以上）を得た。さらにそのまま減圧状態を維持しながら前記リパーゼの共存下でエステル交換反応を９０℃にて２０時間つづけて（Ｒ）−（＋）−１−フェニルエタノール（収率：８７％、物質純度：１００％、光学純度：９９％ｅｅ以上）を減圧蒸留して分離した。
【００２１】
実施例２
アルカリゲネス エスピー（Ａｌｃａｌｉｇｅｎｅｓ ｓｐ．）由来のリパーゼＰＬ（名糖産業（株）製）５ｇ、（Ｒ，Ｓ）−１−（ｐ−クロロフェニル）エタノール５０ｇおよび２，２−ジメチル−１，３−プロパンジオールのパルミチン酸ジエステル（２，２−ジメチル−１，３−プロパンジオールとパルミチン酸とを実施例１記載の方法でエステル化反応させて得たもの。純度：９９％。）２７０ｇを５００ｍｌセパラブルフラスコに入れ、８５℃で超音波発生装置（実施例１と同じ）を用いて４５ｋＨｚ で１分間超音波を照射した。その後、８５℃にて攪拌速度３５０ｒｐｍ で攪拌し、常圧状態で２２時間エステル交換反応を行った。実施例１に記載の方法で測定した反応系の水分量：０．０５重量％、リパーゼ粒子のサイズ：９０％以上が２０〜５０μｍであった。反応終了後、反応物をガスクロマトグラフィーで測定したところ、（Ｒ，Ｓ）−１−（ｐ−クロロフェニル）エタノールの４８モル％がパルミチン酸エステルに変換されていた。そのまま反応系内を９０℃、１ｍｍＨｇに減圧して３０分間蒸留し、未反応の（Ｓ）−（−）−１−（ｐ−クロロフェニル）エタノール（収率：９０％、物質純度：１００％、光学純度：９９％ｅｅ以上）を得た。さらにそのまま減圧状態を維持しながら８５℃で前記リパーゼの共存下でエステル交換反応を７０時間つづけて（Ｒ）−（＋）−１−（ｐ−クロロフェニル）エタノール（収率：８０％、物質純度：１００％、光学純度：９９％ｅｅ以上）を減圧蒸留して分離した。
【００２２】
実施例３
実施例１に記載のリパーゼＱＬ３ｇを、（Ｒ，Ｓ）−２−オクタノール５０ｇに入れ、室温で超音波発生装置（実施例１と同じ）を用いて４５ｋＨｚ で１分間超音波を照射した。その後、実施例１と同様の方法でエステル合成した１，３−プロパンジオールのステアリン酸ジエステル（純度：９９％）２７０ｇを加えて５００ｍｌセパラブルフラスコで１０５℃にて攪拌速度３５０ｒｐｍ で攪拌し、常圧状態で１２時間エステル交換反応を行った。実施例１に記載の方法で測定した反応系の水分量：０．０５重量％、リパーゼ粒子のサイズ：９５％以上が２０〜５０μｍであった。反応終了後、反応物をガスクロマトグラフィーで測定したところ、（Ｒ，Ｓ）−２−オクタノールの５２モル％がステアリン酸エステルに変換されていた。そのまま反応系内を１０５℃、３ｍｍＨｇに減圧して１０分間蒸留し、未反応の（Ｓ）−（＋）−２−オクタノール（収率：８８％、物質純度：１００％、光学純度：９９％ｅｅ以上）を得た。さらにそのまま減圧状態を維持しながら１１０℃で前記リパーゼの共存下にエステル交換反応を２４時間つづけて（Ｒ）−（−）−２−オクタノール（収率：９７％、物質純度：１００％、光学純度：９７％ｅｅ）を減圧蒸留して得た。
【００２３】
実施例４
実施例３において、１，３−プロパンジオールに代えて２，２−ジエチル−１，３−プロパンジオール、２−メチル−２−ｎ−プロピル−１，３−プロパンジオールおよび２−エチル−２−ｎ−ブチル−１，３−プロパンジオールを用い、それぞれ（Ｒ，Ｓ）−２−オクタノールを同様に処理したところ、分離した（Ｓ）−（＋）−２−オクタノールおよび（Ｒ）−（−）−２−オクタノールの収率：８９〜９５％、物質純度：いずれも１００％、光学純度：９７〜９９％ｅｅ以上であった。
【００２４】
比較例１
実施例１において、１，３−プロパンジオールのオレイン酸ジエステルに代えてｎ−プロパノールのオレイン酸モノエステル２７０ｇを用いて同様に処理し、エステル交換反応物を同条件で減圧蒸留したところ、留出物にはｎ−プロパノールが混在し、（Ｓ）−（−）−１−フェニルエタノールの収率：１００％、物質純度：８０％、光学純度：７１％ｅｅであった。さらに減圧蒸留後の残分を同条件下で処理したが留出物は得られなかった。
【００２５】
【発明の効果】
本発明によれば、ラセミ体アルコールと１，３−プロパンジオール類の脂肪酸エステルとを、耐熱性リパーゼの共存下に高温でエステル交換（アルコリシス）反応を行わせるため、該反応が短時間に速やかに進行し、鏡像異性体の一方を簡単に高純度かつ高収率で得ることができる。さらに前記鏡像異性体の一方を分離した残分をそのまま減圧状態で同様にエステル交換（アルコリシス）反応させるため、鏡像異性体の他方が再び遊離し、該反応を行いながら同時に前記鏡像異性体の他方をも高純度かつ高収率で得ることができ、その製造工程は簡略化される。[0001]
[Industrial application fields]
The present invention relates to a method for producing optically active alcohols that are important as raw materials for pharmaceuticals, agricultural chemicals, etc. or intermediates for raw materials and synthetic intermediates for fine chemicals such as liquid crystals.
[0002]
[Prior art]
Optically active alcohols are important substances as raw materials for pharmaceuticals, agricultural chemicals, etc. or intermediates, and synthetic intermediates in the field of fine chemicals such as ferroelectric liquid crystals. However, the purity of the substance itself is necessary to develop sufficient physiological activity and properties. In addition, a considerably high accuracy is required for both optical purity and optical purity. On the other hand, in a reaction using an enzyme such as lipase, lipoprotein lipase, or esterase, it is possible to identify an enantiomer that is difficult to obtain by a chemical reaction involving a normal high temperature. For this reason, the enzyme reaction is useful as a means for increasing optical purity, that is, optical resolution. In recent years, methods for producing optically active alcohols using this enzymatic reaction have been intensively studied.
[0003]
However, the enzyme reaction currently being carried out must be carried out for a very long time of several days to several tens of days (for example, Japanese Patent Laid-Open Nos. 62-166898, 63-273499 and 2). -86797 publications). Moreover, the temperature range in which the enzyme reaction can be performed is at most about 20 to 70 ° C., preferably 30 to 50 ° C. when lipase is used. For example, is the ester transesterified with racemic alcohol in a liquid state in that temperature range? It must be dissolved in a solvent and reacted (Japanese Patent Laid-Open Nos. 62-166898, 63-284184, 2-282340, and 4-349894).
[0004]
Therefore, the ester to be transesterified and the racemic alcohol often have physical properties such as boiling point and melting point that are almost similar, and are usually reactants containing various components such as unreacted substances and by-products. As a purification means for efficiently separating and recovering the target substance from among them and increasing the substance purity and optical purity, it is difficult to use the difference in physical properties, and other complicated and expensive processes must be performed. In other words, after the transesterification reaction is completed, in order to recover the target optically active alcohol from the reaction product, further treatment such as hydrolysis reaction is required, and azeotropic distillation, molecular distillation or preparative liquid chromatography is used. In fact, it is the fact that the substance purity is increased.
[0005]
[Problems to be solved by the invention]
As described above, the current optically active alcohol production method has a drawback that the enzyme reaction must be performed for a very long time. Furthermore, since the enzyme reaction temperature is substantially limited to 30 to 50 ° C. and a suitable raw material is selected, it is difficult to use differences in physical properties such as melting point and boiling point in the separation and purification process of the target product after the reaction. However, there is a problem that a complicated method and means must be selected, and an excessive cost is required to efficiently recover the target optically active alcohol from the reaction product. Accordingly, the present invention provides a method for producing an optically active alcohol utilizing transesterification, whereby an enzymatic reaction can be carried out in a short time, the target product can be easily separated and purified, and the optically active alcohol production process is simplified. The aim was to develop such a method as possible.
[0006]
[Means for Solving the Problems]
The present inventors have intensively studied to solve the above problems and obtain an optically active alcohol by an industrially simple and advantageous method. As a result, racemic alcohol and a specific ester are subjected to transesterification (alcolysis) reaction at a high temperature in the presence of heat-resistant lipase, and more preferably, the reaction is carried out twice, thereby allowing racemic alcohol to occur. Thus, it was found that the optically active alcohol can be efficiently divided, and the present invention has been completed.
[0007]
That is, the gist of the present invention is that a racemic alcohol, a fatty acid ester having 16 or more carbon atoms of 1,3-propanediol having an alkyl group substituted or unsubstituted at the 2-position carbon, a solvent in the presence of a heat-resistant lipase. A transesterification reaction is performed at 81 ° C. or higher under conditions that do not use and substantially do not contain moisture, and are divided into optically active alcohols rich in either the R-form or the S-form. It exists in the manufacturing method of high purity optically active alcohol. An example of a preferred embodiment is that after the transesterification reaction is completed, one of the enantiomers is recovered by distillation under reduced pressure, and further subjected to a transesterification reaction under the same conditions while maintaining the reduced pressure state. This is a process for producing a high-purity optically active alcohol in which the other enantiomer produced and released is recovered by distillation under reduced pressure.
[0008]
In the present invention, the racemic alcohol for optical resolution is not particularly limited, but 2-alkanol is easily resolved, and preferably the following general formula (1)
[Chemical formula 5]

General formula (1)
[In the formula (1), A ≠ B, and A is a phenyl group or the following general formula (2)
[Chemical 6]

General formula (2)
(In formula (2), D ₁ , D ₂ , D ₃ , D ₄ and D ₅ are substituents represented by a halogen atom, an alkyl group having 1 to 3 carbon atoms or an alkoxy group having 1 to 3 carbon atoms) , B is a racemic alcohol represented by an alkyl group having 1 to 3 carbon atoms, CF ₃ or CN], the optical resolution can be efficiently performed by the method of the present invention described below.
[0009]
Specifically, 2-butanol, 2-pentanol, 2-hexanol, 2-heptanol, 2-octanol, 2-nonanol, 2-decanol, 1-phenylethanol, 1-phenyl-1-propanol, ethyl-3- Hydroxy-butanate, ethyl-3-hydroxy-propionate, methyl-3-hydroxy-pentanate, 1-phenyl-1,3-propanediol, 2-phenyl-1-cyclohexanol, 1-pentin-3-ol, 1- (2-bromophenyl) ethanol, 1-parachlorophenylethanol, 1- (4-chlorophenyl) ethanol, 1-chloro-2-octanol, 1,1-difluoro-2-octanol, 1- (2,4-dichlorophenyl) There are racemic alcohols such as ethanol. Of these, 2-octanol, 1-phenylethanol, 1-phenyl-1,3-propanediol, and 2-phenyl-1-cyclohexanol are preferable, and 1-phenylethanol, 2-octanol, (2-bromophenyl) ethanol.
[0010]
The 1,3-propanediol used in the present invention is one in which two identical or different alkyl groups are substituted or unsubstituted at the 2-position carbon, where the alkyl group is a methyl group, an ethyl group, or n-propyl. Group selected from the group consisting of a group, isopropyl group, n-butyl group and sec-butyl group, and specific examples thereof include 1,3-propanediol, 2,2-dimethyl-1,3-propanediol (neopentyl) Glycol), 2,2-diethyl-1,3-propanediol, 2,2-di-n-propyl-1,3-propanediol, 2,2-di-n-butyl-1,3-propanediol, 2- Methyl-2-ethyl-1,3-propanediol, 2-methyl-2-n-propyl-1,3-propanediol, 2-methyl-2-n-butyl-1,3-pro Diol, 2-ethyl-2-n-propyl-1,3-propanediol, 2-ethyl-2-n-butyl-1,3-propanediol, 2-n-propyl-2-n-butyl-1, 3-propanediol etc. can be mention | raise | lifted. Of these, 1,3-propanediol having an unsubstituted alkyl group, 2,2-dimethyl-1,3-propanediol, and 2,2-diethyl-1,3-propanediol are more preferable, and 1,3 -Propanediol is most preferred.
[0011]
The ester used in the present invention refers to an ester of the above 1,3-propanediol and a fatty acid having 16 or more carbon atoms. 1,3-propanediol palmitate, 2-hexyldecanoate, palmitooleate , Stearic acid ester, isostearic acid (2-heptylundecanoic acid, Emery's isostearic acid etc.) ester, oleic acid ester, linoleic acid ester, linolenic acid ester, arachidic acid ester, behenic acid ester, erucic acid ester, lignoceric acid ester Specific examples include serotic acid esters, montanic acid esters, melicic acid esters, and the like. These esters can be used as a mixture in any proportion, and their constituent fatty acids are vegetable oils (soybean oil, rapeseed oil, olive oil, corn oil, safflower oil, sunflower oil, cottonseed oil, palm oil, etc.), animal oils (beef fat) Mixed fats obtained by hydrolyzing fish oil (sardine oil, saury oil, cod liver oil, etc.), and hydrogenated products thereof. Among these, preferred esters are 1,3-propanediol palmitic acid ester, stearic acid ester, oleic acid ester, and behenic acid ester (all of which are linear fatty acid esters), most preferably stearic acid ester and behenic acid ester. It is. Moreover, although it is possible to use either a monoester or a diester, a diester is desirable from the viewpoint of the efficiency of the transesterification reaction. The ester is desirably composed of a linear saturated fatty acid having 18 to 30 carbon atoms, and has a high melting point (preferably 60 ° C. or higher, more preferably 70 ° C. or higher). And Thereby, there exists an advantage which can isolate | separate the target optically active alcohol efficiently from the transesterification product of this invention.
[0012]
The ester to be reacted with the racemic alcohol must be a fatty acid ester of 1,3-propanediol. In the fatty acid ester of a monohydric alcohol, impurities are mixed during the distillation treatment, and a high-purity optically active alcohol is obtained. Absent. When triglyceride is used, the transesterification proceeds, but when the lipase is 1,3 specific, the produced 1,2-type diglyceride is transferred to 1,3-type diglyceride, and decompression operation is performed in the second-stage reaction. However, the optically active alcohol is not liberated again. Furthermore, the reaction rate of the ester of a tetrahydric or higher polyhydric alcohol is extremely reduced.
[0013]
The transesterification reaction of the present invention is characterized by using a heat-resistant lipase. As a result, the transesterification reaction can be carried out quickly while maintaining a high temperature, and further, the transesterification reaction can be carried out at a high temperature and under reduced pressure, and the optical activity generated as a reaction product while the reaction proceeds. Alcohol can be recovered simultaneously.
[0014]
Examples of the heat-resistant lipase include lipases derived from the genus Alcaligenes described in JP-B-58-36953, Rhizopus chinensis described in JP-A-59-156282, and the like. In the present invention, lipase PL-266 produced by Alcaligenes sp. PL-266 (Mikken Kenki No. 3187) described in Japanese Patent Publication No. 58-36953 is disclosed, and Japanese Patent Publication No. 60-15312. The lipase PL-679 produced by Alcaligenes sp. PL-679 (No. 3783 by Mikukenkenbyo) is preferred, and the lipase QL manufactured by Meikatsu Sangyo Co., Ltd. is preferred. Such heat-resistant lipase may be immobilized on a known carrier such as activated carbon, celite, adsorptive resin, ion exchange resin, ceramics, etc., but it is desirable to coexist with the raw material in a powder state as described later.
[0015]
In the transesterification reaction, the racemic alcohol and the ester are mixed as raw materials in a molar ratio of 1: 5 or less, preferably 1: 2-1 based on the racemic alcohol, and a solvent of the raw materials is used. Preferably, the lipase powder is dispersed in a reaction system that is free of water and substantially free of water (ie, the equilibrium water content in the raw material is about 0.1 wt% or less, desirably 0.05 wt% or less). The reaction is carried out with stirring. At this time, it is desirable to carry out the transesterification by controlling 90% or more of the particles of the lipase powder to have a size of 1 to 100 μm, preferably 20 to 50 μm. As a means of aligning the particle size, after dispersing the lipase powder in the raw material heated and dissolved as necessary, ultrasonic treatment, filtration treatment with a precision membrane of the dispersion or ultrafiltration membrane, centrifugal sedimentation treatment, etc. However, it is convenient to irradiate with ultrasonic waves for 1 to 30 minutes, preferably at a reaction temperature or lower, 20 to 150 kHz, and 100 to 250 W.
[0016]
The reaction temperature is set to 81 ° C. or higher, more preferably 91 to 130 ° C., most preferably 101 to 120 ° C., and the first stage when the transesterification (alcolysis in the present invention) reaction is performed once and twice. In this reaction, the reaction rate is checked by, for example, gas chromatography while gently stirring or shaking at normal pressure, and the transesterification reaction is performed for a predetermined time, preferably several hours to 100 hours. . When the reaction temperature is lower than 81 ° C., the reaction proceeds slowly. Conversely, when the reaction temperature exceeds 130 ° C., lipase is deactivated. By this reaction, one of the enantiomers (R-form or S-form) of racemic alcohol is transesterified with the fatty acid ester of 1,3-propanediol (alcolysis), and either of R-form or S-form is obtained. This produces a fatty acid ester of an optically active alcohol and an unreacted optically active alcohol. The transesterification reaction product containing such components is obtained by distilling off the unreacted optically active alcohol in a reduced pressure state (5 to 1 mmHg) without removing or removing the heat-resistant lipase from this, and by transesterifying the optically active product. The other optically active alcohol can be obtained by separating the fatty acid ester of alcohol by a known method such as fractionation, recrystallization, silica gel column chromatography, and the like, followed by acid or alkali hydrolysis. In the present invention, the R-form and S-form optically active alcohols can thereby be highly purified.
[0017]
In the present invention, the embodiment described below is more preferable, and this makes it possible to easily obtain a high-purity product of each of the R-form and S-form optically active alcohols from the racemic alcohol in a high yield. That is, a racemic alcohol and a fatty acid ester having a carbon number of 16 or more of 1,3-propanediol having an alkyl group substituted or unsubstituted at the 2-position carbon are first subjected to the same conditions as described above, ie, in the presence of a heat-resistant lipase. The transesterification reaction (first stage reaction) is carried out at 81 ° C. or higher under normal pressure without using any water, and after the completion of the reaction, unreacted R-form or S The optically active alcohol rich in either of the body is separated by distillation under reduced pressure. As a result, in the residue subjected to the distillation treatment, fatty acid ester of either one of the R-form or S-form which was transesterified (the other of the enantiomers not distilled under reduced pressure) was used as a raw material. , A component in which a fatty acid ester of 3-propanediol is partially or completely alcoholically decomposed coexists.
[0018]
Following the first stage reaction, in the second stage reaction, the residue is maintained under reduced pressure (5 to 1 mmHg) as it is, under the same conditions as the first stage reaction (in the presence of a heat-resistant lipase, solvent-free and substantially The reaction is carried out at a temperature of 81 ° C. or higher under the conditions of mechanical anhydrous, and the optically active alcohol of either the R-form or S-form produced by the reaction is desirably reacted while the reaction is being carried out. After completion, it is separated by distillation under reduced pressure. Here, the heat-resistant lipase can be conveniently added to the reaction product as it is in the first-stage reaction to cause the second-stage reaction to be performed, but may be newly added at the start of the second-stage reaction.
Thus, the optically active alcohols of high purity R-form and S-form can be easily separated from the racemic alcohol with high yield.
[0019]
【Example】
The substance purity of the compounds obtained in the following examples and comparative examples was determined by gas chromatography (manufactured by Shimadzu Corporation, GC-14A), and the optical purity was determined by measuring the specific rotation with a polarimeter (JASCO ( It was measured by using DIP-370), and the measured value was calculated by comparing with the value of the standard sample.
[0020]
Example 1
3 g of lipase QL derived from Alcaligenes sp. (Manufactured by Meika Sangyo Co., Ltd.), 50 g of (R, S) -1-phenylethanol and 1,3-propanediol oleic acid diester (1,3-propane Diol and oleic acid were obtained by esterification reaction at 150 to 200 ° C. for 5 hours using p-toluenesulfonic acid as a catalyst. Purity: 99%.) 270 g was placed in a 500 ml separable flask and ultrasonicated at room temperature. Ultrasonic waves were irradiated for 1 minute at 45 kHz using a generator (manufactured by Shimadzu Corporation, SUS-103). Thereafter, the mixture was stirred at 90 ° C. at a stirring speed of 350 rpm, and a transesterification reaction was performed for 24 hours under normal pressure. Water content in the reaction system (Karl Fischer method): 0.05% by weight, size of lipase particles (particle size distribution measuring device manufactured by Coulter Electronics Co., Ltd .: measurement with Multisizer): 95% or more was 20 to 50 μm. After completion of the reaction, the reaction product was measured by gas chromatography. As a result, 49 mol% of (R, S) -1-phenylethanol was converted to an oleate. The reaction system was reduced in pressure to 90 ° C. and 1 mmHg and distilled for 20 minutes, and unreacted (S)-(−)-1-phenylethanol (yield: 98%, substance purity: 100%, optical purity: 99 % Ee or higher). Further, the transesterification reaction was continued at 90 ° C. for 20 hours in the presence of the lipase while maintaining the reduced pressure state as it was, and (R)-(+)-1-phenylethanol (yield: 87%, substance purity: 100%). , Optical purity: 99% ee or higher) was separated by distillation under reduced pressure.
[0021]
Example 2
5 g of lipase PL (manufactured by Meisei Sangyo Co., Ltd.) derived from Alcaligenes sp., 50 g of (R, S) -1- (p-chlorophenyl) ethanol and 2,2-dimethyl-1,3-propanediol 500 ml separable flask of 270 g of palmitic acid diester (obtained by esterification of 2,2-dimethyl-1,3-propanediol and palmitic acid by the method described in Example 1. Purity: 99%) Then, ultrasonic waves were applied at 85 kHz for 1 minute at 85 ° C. using an ultrasonic generator (same as in Example 1). Thereafter, the mixture was stirred at 85 ° C. and a stirring speed of 350 rpm, and a transesterification reaction was performed for 22 hours under normal pressure. The water content of the reaction system measured by the method described in Example 1 was 0.05% by weight, and the size of lipase particles: 90% or more was 20 to 50 μm. When the reaction product was measured by gas chromatography after the completion of the reaction, 48 mol% of (R, S) -1- (p-chlorophenyl) ethanol was converted to a palmitate ester. The reaction system was directly reduced in pressure to 90 ° C. and 1 mmHg and distilled for 30 minutes, and unreacted (S)-(−)-1- (p-chlorophenyl) ethanol (yield: 90%, substance purity: 100%, Optical purity: 99% ee or higher) was obtained. Further, the transesterification reaction was continued for 70 hours in the presence of the lipase at 85 ° C. while maintaining the reduced pressure state, and (R)-(+)-1- (p-chlorophenyl) ethanol (yield: 80%, substance purity). : 100%, optical purity: 99% ee or higher) was separated by distillation under reduced pressure.
[0022]
Example 3
3 g of lipase QL described in Example 1 was put into 50 g of (R, S) -2-octanol, and irradiated with ultrasonic waves at 45 kHz for 1 minute at room temperature using an ultrasonic generator (same as in Example 1). Thereafter, 270 g of 1,3-propanediol stearate diester (purity: 99%) synthesized by the same method as in Example 1 was added, and the mixture was stirred in a 500 ml separable flask at 105 ° C. with a stirring speed of 350 rpm. Transesterification was performed for 12 hours under pressure. The water content of the reaction system measured by the method described in Example 1 was 0.05% by weight, and the size of lipase particles: 95% or more was 20 to 50 μm. After completion of the reaction, the reaction product was measured by gas chromatography. As a result, 52 mol% of (R, S) -2-octanol was converted to stearic acid ester. The reaction system was reduced in pressure to 105 ° C. and 3 mmHg for 10 minutes, and unreacted (S)-(+)-2-octanol (yield: 88%, substance purity: 100%, optical purity: 99%) ee or higher). Furthermore, the transesterification reaction was continued for 24 hours at 110 ° C. in the presence of the lipase while maintaining the reduced pressure state as it was, and (R)-(−)-2-octanol (yield: 97%, substance purity: 100%, optical) Purity: 97% ee) was obtained by distillation under reduced pressure.
[0023]
Example 4
In Example 3, instead of 1,3-propanediol, 2,2-diethyl-1,3-propanediol, 2-methyl-2-n-propyl-1,3-propanediol and 2-ethyl-2- When (R, S) -2-octanol was similarly treated with n-butyl-1,3-propanediol, the separated (S)-(+)-2-octanol and (R)-(- ) -2-Octanol yield: 89-95%, substance purity: all 100%, optical purity: 97-99% ee or more.
[0024]
Comparative Example 1
In Example 1, 270 g of oleic acid monoester of n-propanol was used instead of oleic acid diester of 1,3-propanediol, and the transesterification product was distilled under reduced pressure under the same conditions. The product was mixed with n-propanol, and the yield of (S)-(−)-1-phenylethanol was 100%, the substance purity was 80%, and the optical purity was 71% ee. Further, the residue after distillation under reduced pressure was treated under the same conditions, but no distillate was obtained.
[0025]
【The invention's effect】
According to the present invention, a racemic alcohol and a fatty acid ester of 1,3-propanediol are subjected to a transesterification (alcolysis) reaction at a high temperature in the presence of a heat-resistant lipase. And one of the enantiomers can be easily obtained in high purity and high yield. Furthermore, since the residue obtained by separating one of the enantiomers is subjected to a transesterification (alcolysis) reaction in the same manner under reduced pressure, the other of the enantiomers is liberated again, and the other of the enantiomers is simultaneously subjected to the reaction. Can be obtained with high purity and high yield, and the manufacturing process is simplified.

Claims (7)

A racemic alcohol of a compound represented by 2-alkanol or the following general formula (1), and a fatty acid ester having 16 or more carbon atoms of 1,3-propanediol, in which an alkyl group is substituted or unsubstituted at the 2-position carbon, In the presence of a heat-resistant lipase derived from the genus Alcaligenes, a transesterification reaction is performed at 81 ° C. or higher without using a solvent and substantially free of moisture. A method for producing a high-purity optically active alcohol, characterized in that it is divided into optically active alcohols rich in one of them.

General formula (1)
[In formula (1), A ≠ B, A is a phenyl group or the following general formula (2) (in formula (2), D ₁ , D ₂ , D ₃ , D ₄ and D ₅ are halogen atoms or carbon atoms 1 to 3 alkyl groups or alkoxy groups having 1 to 3 carbon atoms), and B is an alkyl group having 1 to 3 carbon atoms.

General formula (2) A racemic alcohol of a compound represented by 2-alkanol or a compound represented by the following general formula (1), and a fatty acid ester having 16 or more carbon atoms of 1,3-propanediol in which an alkyl group is substituted or unsubstituted at the 2-position carbon; In the presence of a heat-resistant lipase derived from the genus Alcaligenes, a transesterification reaction is performed at 81 ° C. or higher without using a solvent and substantially free of moisture. The optically active alcohol rich in either R-form or S-form was recovered by distillation under reduced pressure, and then the residue obtained by distillation under reduced pressure was maintained in a reduced pressure state as in the above , and heat resistant from the genus Alcaligenes as described above. A transesterification reaction at 81 ° C. or higher under solvent-free and substantially anhydrous conditions. Preparation of highly pure optically active alcohol, which comprises recovering the optically active alcohol rich in either one of the R or S is released.

General formula (1)
[In formula (1), A ≠ B, and A is a phenyl group or the following general formula (2) (in formula (2), D ₁ , D ₂ , D ₃ , D ₄ and D ₅ are halogen atoms or carbon atoms 1 to 3 alkyl groups or C1 to C3 alkoxy groups), and B is an alkyl group having 1 to 3 carbon atoms.

General formula (2) The method for producing a high purity optically active alcohol according to claim 1 or 2, wherein the 2-position carbon of 1,3-propanediol is unsubstituted with an alkyl group . The method for producing a high purity optically active alcohol according to any one of claims 1 to 3, wherein the fatty acid is a linear saturated fatty acid having 18 or more carbon atoms . The method for producing a high-purity optically active alcohol according to any one of claims 1 to 4, wherein the heat-resistant lipase derived from the genus Alcaligenes is a lipase derived from Alcaligenes sp. The method for producing a high-purity optically active alcohol according to any one of claims 1 to 5, wherein the heat-resistant lipase derived from the genus Alcaligenes is in a powder form and 90% or more of the particles have a particle diameter of 1 to 100 µm. . The method for producing a high purity optically active alcohol according to any one of claims 1 to 6, wherein the reaction temperature is 101 to 120 ° C.