JPS595575B2 - Hydroxylamine stabilizer - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hydroxylamine stabilizer comprising quinoline represented by the following general formula.

00 (wherein, R1 represents an amino group, a hydroxyl group, or a lower alkoxy group, when R1 is an amino group, R2 is a hydrogen atom, when R1 is a hydroxyl group, R2 is a sulfonic acid group, and when R1 is a lower alkoxy group) (R2 represents a hydrogen atom) Hydroxylamine and its salts are used in anti-oxidation, textile treatment, dyeing industry, natural color photography, rubber industry, oil and fat industry, pharmaceutical synthesis, agricultural chemical synthesis, etc. In recent years, in particular, they have been used as raw materials for organic synthesis. Its weight is increasing.

Hydroxylamine is an extremely unstable base with a melting point of 33.05°C, and its 4.06Mol/L aqueous solution is
By keeping it for 44 hours, 79.7% decomposition was observed.

However, the aqueous solution of the salt is extremely stable, 5Mol/L, ゛3
Even after one month of standing at 0°C, the decomposition was within the measurement error. Therefore, it is commercially available as a stable sulfate, hydrochloride, or nitrate. Thus, many of these applications do not require hydroxylamine salts, but rather free hydroxylamine. Conventionally, hydroxylamine is generally used as hydroxylamine by neutralizing it with an alkali in a solvent containing a substance that is likely to react with the hydroxylamine salt. As the reaction solvent, organic solvents such as alcohols are generally used.

That is, the substance to be reacted is dissolved in a solvent, hydroxylamine sulfate crystals are dissolved in the solution, and an alcoholic solution containing NaOH is gradually added while stirring to cause the reaction. In this case, a film of fine crystals of Na2sO4, which is insoluble in alcohol, is formed on the surface of solid hydroxylamine sulfate, which prevents the alcohol solution of NaOH from reaching the hydroxylamine sulfate crystals. At the end of the reaction, unused hydroxylamine sulfate particles remain covered with a thick Na2sO4 film. In actual factory operations, unused hydroxylamine sulfate can reach as much as 10%. Furthermore, in order to prevent pollution, it becomes necessary to remove these unused substances by oxidizing them using an oxidizing agent. In addition, due to the fine crystals of Na2sO4 formed in the alcohol solvent at the end of the reaction, the entire reaction solution became porridge-like.
There is also a large loss of active ingredients when the crystals are deliquified.

Almost the same results can be obtained by using hydroxylamine hydrochloride or hydroxylamine nitrate in place of hydroxylamine sulfate. The present invention provides a stabilized hydroxylamine by adding a quinoline stabilizer.

As can be seen from Tables 1, 2, 3 and 4, quinolines contain only 1/1000 times the number of moles of hydroxylamine and keep hydroxylamine extremely stable with almost no decomposition. Further, by using the stable hydroxylamine according to the present invention in the reaction, reaction inhibiting substances such as Na2sO4 are not crystallized, so that the reaction can be carried out using a concentrated solution.

Furthermore, since crystals such as Na2sO4 do not crystallize, centrifugation can be eliminated, eliminating loss of reaction products and solvent.
Therefore, it has many advantages such as increased capacity due to the same general equipment and rationalization of manpower and processes. Next, examples will be shown. Example
1 Dissolve JIS K8993 hydroxylamine sulfate reagent special grade in pure water to make about 5M01/L solution.

This is called liquid A. Dissolve JIS K8576 NaOH reagent special grade in pure water to make an approximately 50% solution. This is called liquid B. Next, liquid A was cooled to 5°C, and B, which had been previously cooled to 5°C, was
Neutralize with liquid. Neutralization was carried out at a temperature of 0° C. to 10° C. with strong stirring, and the completion of neutralization was measured by the JIS Z88O2 glass electrode method, with pH 8.5 as the end point. After neutralization, the liquid was cooled to 0° C. to precipitate Na2SO4.10H20 crystals, which were filtered through a Buchna funnel using filter paper. This is called liquid C. JISK8 hydroxylamine in liquid C
As a result of measurement using the test method of 993, the hydroxylamine content was 4.06 M01/L. This C solution is used as a stock solution,
To this was added various quinolines as stabilizers of the present invention in an amount of 0.001 times the number of moles of hydroxylamine. Then, the content of residual hydroxylamine after being left at 40° C. for 6 hours, 16 hours, and 24 hours was measured. The results were as shown in Table 1. Example 2 Hydroxylamine hydrochloride according to JIS K8201 was dissolved in methyl alcohol at 40°C to saturation (approximately 2.7
5M01/L).

This is called liquid D. The same NaOH as in Example 1 was dissolved in methyl alcohol to a concentration of about 5M01/L. This is called liquid E. Next, cool the D solution to 5℃, stir it vigorously and take care not to let the liquid temperature exceed 10℃.
The liquid was added gradually. Then, a large amount of fine NaCl crystals are generated, and the liquid becomes porridge-like. Neutralization was measured using a glass electrode in the same manner as in Example 1, and the end point was set at pH 8.5. After neutralization, the mixture was filtered through a Buchna funnel lined with filter paper. This filtrate is F
Make it into a liquid. The content of hydroxylamine in the F solution was measured in the same manner as in Example 1 and was found to be 1.98 M01/L. Next, liquid F was placed in a round bottom flask under reduced pressure at about 30°C for about 2 hours.
It was concentrated to double the concentration. As a result of measurement in the same manner as in Example 1, the hydroxylamine content was 4.09M0.
It was 1/L. This is called liquid G. Using G solution as the stock solution,
To this was added so that the number of moles was 1/1000 times the number of moles of the stabilizer of the present invention.

The results of testing in the same manner as in Example 1 are shown in Table 2. Example 3 The difference from Example 2 was that ethyl alcohol was used instead of methyl alcohol as a solvent, and the rest was almost the same as Example 2.

However, since the solubility of hydroxylamine hydrochloride in ethyl alcohol is poor, the concentration of hydroxylamine before concentration was slightly diluted, and therefore the degree of concentration was slightly increased. The concentration of this hydroxylamine was 3.96 M01/L. The results of testing in the same manner as in Example 1 are shown in Table 3. Example 4 The only difference from Example 1 was the neutralization point.

One of the two samples had a pH of 6. The Ol hydroxylamine concentration was 4.00 M01/L, and the other pH was 7. The concentration of Ol hydroxylamine was 4.03 M01/L.

Then, a 24-hour standing test was carried out in the same manner as in Example 1, and the results were as shown in Table 4. For comparison, some of the results of Example 1 are also rewritten.

Claims (1)

[Claims] 1. A stabilizer for hydroxylamine consisting of quinoline represented by the following general formula ▲ Numerical formulas, chemical formulas, tables, etc. are available ▼ (In the formula, R_1 represents an amino group, a hydroxy group, or a lower alkoxy group) , when R_1 is an amino group, R_2 is a hydrogen atom; when R_1 is a hydroxyl group, R_2 is a sulfonic acid group; when R_1 is a lower alkoxy group, R_2 is a hydrogen atom).