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A kind of preparation method of 1-methylimidazole

A technology of methyl imidazole and methyl group, which is applied in the field of preparation of 1-methyl imidazole, can solve the problems of low yield and the like, and achieve the effects of reducing production cost, being easy to promote in large-scale industrialization, and having a simple preparation method.

Active Publication Date: 2018-09-14
NINGXIA JOIE MATERIAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The technical problem to be solved in the present invention is to provide a kind of preparation method of 1-methylimidazole, to solve the problem that the productive rate that prior art exists is lower

Method used

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  • A kind of preparation method of 1-methylimidazole
  • A kind of preparation method of 1-methylimidazole
  • A kind of preparation method of 1-methylimidazole

Examples

Experimental program
Comparison scheme
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Embodiment 1

[0027] Raw materials and their mole fractions: 1 part of 2-chloro-2-(((methylamino)methyl)imino)ethyl triflate, 3.5 parts of ethanol, 2.5 parts of hydrogen chloride, 0.2 part of glacial acetic acid, 4 parts of sodium hydroxide (existing at a concentration of 2 mol / L in water); wherein, except for aqueous sodium hydroxide solution, all raw materials need to be dehydrated first.

[0028] Preparation:

[0029] (1) Dissolve 2-chloro-2-(((methylamino)methyl)imino)ethyl triflate in ethanol, stir at 4°C for 8 hours and set aside;

[0030] (2) Pass hydrogen chloride gas into the mixed system obtained in step (1), react at 20°C for 5h under airtight conditions, add glacial acetic acid, and stir at 4°C for 2h;

[0031] (3) Add aqueous sodium hydroxide solution to the mixed system obtained in step (2), stir and react at 43° C. for 4 h, extract with chloroform, rotary evaporate, and dry to obtain 1-methylimidazole.

Embodiment 2

[0033] Raw material and preparation method are the same as embodiment 1, difference is, no longer add glacial acetic acid in the step (2).

Embodiment 3

[0035] The raw materials and preparation method are the same as those in Example 1, except that the ethanol in step (2) is an aqueous ethanol solution with a volume fraction of 80%.

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Abstract

The invention discloses a preparation method of 1-methylimidazole obtained by firstly carrying out ring formation of 2-chloro-2-(((methylamino)methyl)imino)ethyl trifluoromethanesulfonate and then forming a double bond. Compared with the prior art, a by-product obtained in other process production lines is used as a raw material, so that the production cost is greatly reduced, and the productive rate can reach 91% and is far higher than that of a conventional process. At the same time, the preparation method is simple, and is prone to large-scale industrialized promotion.

Description

technical field [0001] The invention belongs to the field of chemical synthesis, and in particular relates to a preparation method of 1-methylimidazole. Background technique [0002] 1-Methylimidazole is an important intermediate substance in the field of medicine and chemical industry. It is mainly used in the synthesis of deoxyribonucleic acid and the synthesis of glycolylation catalysts. At the same time, it can also be used as a curing agent for epoxy resin and other resins, used in pouring, bonding and glass fiber reinforced plastics and other fields. [0003] At present, although the process for preparing 1-methylimidazole in the market is relatively mature, its cost and yield are not satisfactory. Therefore, develop a kind of high yield, the preparation method of the 1-methylimidazole of low cost has broad market prospect. Contents of the invention [0004] The technical problem to be solved by the present invention is to provide a preparation method of 1-methyli...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D233/58
CPCC07D233/58
Inventor 李明梅孙新赵春霞
Owner NINGXIA JOIE MATERIAL CO LTD