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Synthesis method of N-methyl-2-hydroxyethyl hydroxyethyl

A technology of hydroxyethylpyrrolidine and a synthesis method, applied in directions such as organic chemistry, can solve problems such as high production cost and low yield, and achieve the effects of short synthesis route, mild reaction conditions and high industrial production value

Active Publication Date: 2010-06-16
江苏恒祥化学股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0008] The technical problem to be solved by the present invention is to overcome the problems of high production cost and low yield in the existing synthetic method of N-methyl-2-hydroxyethylpyrrolidine, and provide a new N-methyl-2-hydroxyethylpyrrolidine - a synthetic method for 2-hydroxyethylpyrrolidine, which has the advantages of simple and convenient steps, lower production cost and high yield

Method used

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  • Synthesis method of N-methyl-2-hydroxyethyl hydroxyethyl
  • Synthesis method of N-methyl-2-hydroxyethyl hydroxyethyl
  • Synthesis method of N-methyl-2-hydroxyethyl hydroxyethyl

Examples

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Embodiment 1

[0029] Take a 1000ml three-neck flask, add 140ml of dimethyl sulfate and 140ml of N-methylpyrrolidone, raise the temperature to 60°C, and keep the temperature at 60-75°C for 3 hours. After completion, cool to 5°C, add 145ml of ethyl cyanoacetate dropwise, and react below 20°C for 3 hours, filter, and dry to obtain about 240g of intermediate (I), with a yield of 86.7%.

Embodiment 2

[0031] Take a 1000ml three-neck flask, add 140ml dimethyl sulfate and 140ml N-methylpyrrolidone, raise the temperature to 50°C, and keep it at 50-60°C for 3 hours. After completion, cool to 5°C, add 145ml of ethyl cyanoacetate dropwise, and react below 20°C for 3 hours, filter, and dry to obtain about 205g of intermediate (I), with a yield of 74.0%.

Embodiment 3

[0033] Take a 1000ml three-neck flask, add 140ml of dimethyl sulfate and 140ml of N-methylpyrrolidone, raise the temperature to 75°C, and keep it at 75-80°C for 3 hours. Finished, then cooled to 5°C, added dropwise 145ml of ethyl cyanoacetate, after dropping, reacted below 20°C for 3 hours, filtered, and dried to obtain about 130g of intermediate (I), with a yield of 46.9%.

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Abstract

The invention discloses a synthesis method of N-methyl-2-hydroxyethyl hydroxyethyl, which comprises the following steps of: (1) adding dimethyl sulfate and N-methyl pyrrolidone into a reaction kettle for reaction; (2) cooling and dropwise adding an ethanol solution of sodium ethylate, continuously dropwise adding ethyl cyanoacetate, reacting and filtering to obtain an intermediate (I); (3) adding the intermediate (I) and a catalyst as well as a high-boiling point organic solvent to the reaction kettle, heating, fractionating, reacting, filtering, recovering propylene glycol, and carrying vacuum rectification to obtain a intermediate (II); and (4) adding the intermediate (II) and the catalyst as well as a solvent into the reaction kettle, replacing by using nitrogen and hydrogen sequentially, introducing hydrogen, reacting, cooling, evacuating, filtering, evaporating out moisture content, and carrying out vacuum rectification to obtain the N-methyl-2-hydroxyethyl hydroxyethyl. The synthesis method has the advantages of cheap and easily obtained raw materials, short synthesis route, mild reaction conditions, relatively low production cost and higher overall yield.

Description

technical field [0001] The invention relates to a synthesis method of pyrrolidine, in particular to a synthesis method of N-methyl-2-hydroxyethylpyrrolidine, and belongs to the field of synthesis of pyrrolidine. Background technique [0002] N-methyl-2-hydroxyethylpyrrolidine is a colorless and transparent liquid with amino compounds, which is mainly used in the preparation of antipsychotic and antiviral drugs. [0003] Mainly disclose the synthetic routes of A, B and C total 3 kinds of N-methyl-2-(β-hydroxyethyl) pyrrolidines in the prior art (see figure 1 , figure 2 with image 3 ). In the above three synthetic routes, side chain reaction is involved, which is their common point and the core of synthesizing the subject compound. The side chain reaction of vinyl acetate on the pyrrolidine ring or pyrrolidone ring is a typical free radical addition reaction, and the yields are: route A: 86%, route B: 78%, route C: 67%. For C, due to the N-CH 3 A similar reaction can t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D207/08
Inventor 邱志刚
Owner 江苏恒祥化学股份有限公司
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