Method for preparing acetaldoxime

A technology of acetaldehyde oxime and acetaldehyde, applied in the field of organic chemical synthesis, can solve the problems of large amount of hydroxylamine salt, generation of by-products, long reaction process, etc., achieve high conversion rate, reduce pollution, and simple reaction process

Inactive Publication Date: 2013-06-26
EAST CHINA NORMAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, acetaldehyde oxime is generally produced by the aminoxime compound method of sulfuric acid (hydrochloride) hydroxylamine and acetaldehyde. The main disadvantages of this production process are: complex process, long reaction process, large amount of hydroxylamine salt, and need to add alkali to adjust The pH of the reaction system, and by-products are generated, which is not friendly to the environment
[0004] Titanium-silicon molecular sieves are new heteroatom molecular sieves developed in the early 1980s. Currently, the titanium-silicon molecular sieves with microporous structures include TS-1, Ti-Beta, Ti-MOR, Ti-MWW, etc. Titanium-silicon molecular sieves with pore structure include Ti-MCM-41, Ti-MCM-48 and Ti-SBA-15, etc. Because molecular sieves have a porous and orderly structure, they have excellent type selection functions and will have a transition of valence characteristics. Metal titanium is introduced into the molecular sieve framework structure to form oxidation-reduction catalysis, which has been widely used in the ammoximation of aldehydes and ketones, such as Chinese patent: CN 1683323A discloses the preparation of cyclohexanone oxime, CN 1651405A, CN 101318912A discloses the preparation of methyl ethyl ketone oxime with TS-1 and CN 1022416605A discloses the preparation of citronellaldoxime with TS-1, but there is no patent or literature report to prepare acetaldehyde oxime with titanium silicon molecular sieve,

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0021] a. Preparation of reaction system

[0022] Acetaldehyde, liquid ammonia with a mass concentration of 25%, tert-butanol and a catalyst in a mass ratio of 1:0.46:5:0.1 were stirred and mixed in a reactor to form a reaction system. The catalyst was Ti-MOR titanium silicon molecular sieve.

[0023] b, the synthetic reaction of acetaldehyde oxime

[0024] Heat the above reaction system, when the temperature of the reactor rises to 60°C, add hydrogen peroxide with a mass concentration of 30% to the reaction system dropwise, the mass ratio of hydrogen peroxide to acetaldehyde is 0.93:1, and the dropping time is 1.5 Hours, continue to react for 0.5 hours after the dropwise addition, and the pressure of the reaction system is normal pressure.

[0025] c, the purification of acetaldehyde oxime

[0026] After the above reaction, the catalyst in the reaction system was filtered out, and then the product was purified by distillation to obtain acetaldehyde oxime. The analysis resul...

Embodiment 2

[0028] a. Preparation of reaction system

[0029] Acetaldehyde, liquid ammonia with a mass concentration of 25%, n-propanol and a catalyst are stirred and mixed in a reactor at a mass ratio of 1:0.46:10:0.1 to form a reaction system. The catalyst is Ti-MOR titanium silicon molecular sieve.

[0030] b, the synthetic reaction of acetaldehyde oxime

[0031] Heat the above reaction system, when the temperature of the reactor rises to 60°C, add hydrogen peroxide with a mass concentration of 30% to the reaction system dropwise, the mass ratio of hydrogen peroxide to acetaldehyde is 0.93:1, and the dropping time is 1.5 Hours, continue to react for 0.5 hours after the dropwise addition, and the pressure of the reaction system is normal pressure.

[0032] c, the purification of acetaldehyde oxime

[0033] After the above reaction was finished, the catalyst in the reaction system was filtered out, and then the product was purified by distillation to obtain acetaldehyde oxime. The anal...

Embodiment 3

[0035] a. Preparation of reaction system

[0036] Acetaldehyde, liquid ammonia with a mass concentration of 25%, isopropanol, and a catalyst are stirred and mixed in a reactor at a mass ratio of 1:0.46:5:0.25 to form a reaction system. The catalyst is Ti-MOR titanium silicon molecular sieve.

[0037] b, the synthetic reaction of acetaldehyde oxime

[0038] Heat the above reaction system, when the temperature of the reactor rises to 60°C, add hydrogen peroxide with a mass concentration of 30% to the reaction system dropwise, the mass ratio of hydrogen peroxide to acetaldehyde is 0.93:1, and the dropping time is 1.5 Hours, continue to react for 0.5 hours after the dropwise addition, and the pressure of the reaction system is normal pressure.

[0039] c, the purification of acetaldehyde oxime

[0040] After the above reaction was finished, the catalyst in the reaction system was filtered out, and then the product was purified by distillation to obtain acetaldehyde oxime. The an...

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PUM

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Abstract

The invention discloses a method for preparing acetaldoxime. The method is characterized by carrying out a high-selectivity acetaldoxime combination reaction on acetaldehyde, ammonia and an alcohol solvent in a liquid phase by taking titanium silicate molecular sieve as a catalyst and taking hydrogen peroxide as an oxidant, and distilling and purifying the reaction solution to acquire the acetaldoxime, wherein the mass ratio of the acetaldehyde, the ammonia, the alcohol solvent and the catalyst is 1: (0.38-0.78): (2-10): (0.05-0.68). Compared with the prior art, the method for preparing the acetaldoxime has the advantages of high conversion rate of acetaldehyde, good selectivity and high utilization rate of hydrogen peroxide; the reaction process is simple and is environment-friendly and pollutions to the environment are reduced; the industrial production is facilitated; and the development of green chemistry is promoted.

Description

technical field [0001] The invention relates to the technical field of organic chemical synthesis, in particular to a method for preparing acetaldehyde oxime. Background technique [0002] Acetaldoxime is a less toxic reducing agent and an important reagent in organic synthesis and analysis. In the 1990s, acetaldehyde oxime replaced the highly toxic hydrazine as a boiler water oxygen scavenger, and its oxygen scavenging effect was much higher than that of hydrazine, so it was widely used. Acetaldoxime is an important intermediate for the synthesis of pesticides methomyl and thiodicarb. These two pesticides are good broad-spectrum insecticides. With the continuous growth of production, the market demand for acetaldehyde oxime also increases . [0003] At present, acetaldehyde oxime is generally produced by the aminoxime compound method of sulfuric acid (hydrochloride) hydroxylamine and acetaldehyde. The main disadvantages of this production process are: complex process, lon...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07C251/38C07C249/04
Inventor 吴鹏丁姜宏徐乐吴静黄仕杰杨玉林吴海虹
Owner EAST CHINA NORMAL UNIV
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