Method for synthesizing methoxy amine hydrochlorate

A technology of methoxyamine hydrochloride and methyl, which is applied in the field of compound synthesis, can solve the problems of high toxicity, pollution, yield drop, and high recycling cost, and achieve the effects of reducing exhaust gas emissions, mild reaction conditions, and reducing investment costs

Inactive Publication Date: 2009-08-12
宁波四明化工有限公司 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This process uses liquid sulfur dioxide and sodium nitrite, which is highly toxic and polluting. At the same time, more than ten tons of waste water containing a large amount of sodium sulfate will be produced to produce a ton of products, and a large amount of nitrogen oxides and other waste gases will be produced. Therefore, it is safe and environmentally friendly. There are certain problems
[0004] Han Shidong et al. (Zhejiang Chemical Industry, 2005, 36(9), 14~16) and Pan Zhongwen et al. (Fine Chemical Intermediates, 2007, 37(6), 17~18, 21) introduced a method using acetone oxime ether and O- The process of synthesizing alkoxyamines by hydrolysis of alkylphthalimides, the hydrolysis of acetone oxime ether requires continuous distillation of acetone in the rectification tower to promote the reaction, and azeotropic dehydrating agents such as toluene, hexane, etc. Organic solvents help dehydration, and it is not easy to control the side reactions in the hydrolysis process, resulting in a decrease in yield and an increase in cost
[0005] Li Wenxia

Method used

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  • Method for synthesizing methoxy amine hydrochlorate
  • Method for synthesizing methoxy amine hydrochlorate
  • Method for synthesizing methoxy amine hydrochlorate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Add 90g of water, 10g (0.25mol) NaOH into a 150mL flask equipped with electric stirring, thermometer, and condenser, stir and dissolve at room temperature, then 8.7g (0.10mol) butanone oxime, 0.3g PEG500, and then cool to 5°C , began to add 16.4g (0.13mol) of dimethyl sulfate, added for 1h, and reacted at 10°C for 4h after the addition was completed. Then cool to below 5°C and let it stand for more than 1 hour, then separate the upper organic layer, that is, the oil layer, to obtain 9.0g; the water layer is heated up and distilled, and the distillate is collected, and the distillation temperature ends when the gas phase temperature reaches 95°C, to obtain 22.3g. Combine the oil layer and distillate, add 22.6g of 30% hydrochloric acid (0.19mol) and mix well.

[0035] Prepare a glass rectification column with an inner diameter of 20mm and a height of 1600mm equipped with spring glass packing. The rectification column is divided into two parts with the same height. There i...

Embodiment 2

[0037] The amount of NaOH was changed to 0.20 mol, and the others were the same as in Example 1. The result was 6.5 g of methoxylamine hydrochloride, the yield was 77.8%, and the product mole fraction was 98.8%.

Embodiment 3

[0039] The water consumption was changed to 45g, and the others were the same as in Example 1. The result was 6.3g of methoxylamine hydrochloride, a yield of 75.4%, and a product mole fraction of 98.7%. .

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Abstract

The invention discloses a synthesizing method of methoxy amine hydrochloride. Butanone oxime, water, sodium hydroxide, phase transfer catalyst are added in a reaction container; the temperature is decreased to 0-15 DEG C; a methylating reagent begins to be added; then, reaction is carried out at a temperature of 5-120 DEG C for 3-6 h; standing and layering are carried out so that an organic layer O-methyl-2-diacetylmonoxime ether and a water layer are separated; then, the O-methyl-2-diacetylmonoxime ether in the water layer is distilled and recovered under the normal pressure; the separated O-methyl-2-diacetylmonoxime ether is mixed with the distilled and recovered O-methyl-2-diacetylmonoxime ether and then with hydrochloric acid solution with a mass percentage of 30-35 percent; the mixed solution undergoes feeding and rectification at the middle of a rectifying column; butanone and methanol are recovered by the column top; methoxy amine hydrochloride solution is recovered by the column bottom; and the methoxy amine hydrochloride solution also undergo evaporation and dehydration by heating so as to obtain a hydrochloride concentrated solution thereof. The synthesizing method is simple, generates a small amount of three wastes and improves the operation environment and the yield rate.

Description

technical field [0001] The invention relates to the technical field of compound synthesis methods, in particular to a method for synthesizing methoxyamine hydrochloride. Background technique [0002] Methoxylamine hydrochloride, also known as o-methylarginine hydrochloride, is an important chemical product and pharmaceutical intermediate, which can be used in color photography and film printing, as a reducing agent in the organic synthesis industry to prepare oximes, and in medicine. Used in the production of sulfamethoxazole, ethinoxazole, hydroxyurea, cefuroxime, etc. [0003] The methods currently used for the synthesis of methoxyamine hydrochloride include: Ji Yongxin (Chemistry and Adhesion, 2001, 5, 200-202) introduced such a synthetic route: use sodium bisulfite and sulfur dioxide to react with sodium nitrite Hydroxylamine sodium sulfite, then methylated, hydrolyzed, neutralized to form a salt. This process uses liquid sulfur dioxide and sodium nitrite, which is hig...

Claims

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Application Information

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IPC IPC(8): C07C239/20
Inventor 张胜建林勇罗署邵振平张连芳
Owner 宁波四明化工有限公司
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