Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for preparing alpha-chloro-alpha-acetyl-gamma-butyrolactone

A technology of acetyl and butyrolactone, applied in the direction of organic chemistry, etc., can solve problems such as low purity and complicated operation, and achieve the effect of simple operation and mild reaction conditions

Inactive Publication Date: 2020-04-17
江西天新药业股份有限公司
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] The purpose of the present invention is to provide a new method capable of preparing α-butyrolactone with high purity in order to overcome the defect that the purity is not high and the operation is complicated in the method for preparing α-chloro-α-acetyl-γ-butyrolactone in the prior art. Chloro-α-acetyl-γ-butyrolactone method

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0038] The preparation method of the invention can significantly improve the purity of the α-chloro-α-acetyl-γ-butyrolactone product, and slightly increase the product yield, laying a solid foundation for further preparation of high-quality VB1.

[0039] The present invention will be described in detail below by way of examples. In the following examples, all raw materials used are commercially available unless otherwise specified.

Embodiment 1

[0041] Take 273g of 15% by weight NaOH aqueous solution, stir and cool down to below 10°C, start to slowly add 128g of α-acetyl-γ-butyrolactone dropwise, cool with ice water, the reaction exotherm is obvious, control the internal temperature at 8-12°C, A large amount of solid sodium salt was precipitated in the late stage of the reaction. After the dropwise addition of α-acetyl-γ-butyrolactone, stir and keep warm for 30 minutes, then add 350g of water to dissolve the precipitate, cool the system to 8°C and slowly introduce chlorine gas to control the reaction The temperature of the liquid is 8-12°C. When the reaction liquid is finally milky white and the pH of the solution is 5.2, end the chlorine flow, nitrogen replacement, vacuum pumping for 10 minutes, let stand and separate layers, and the lower organic phase is α-chloro-α-acetyl Base-γ-butyrolactone, the gas phase content is 99.6%, and the molar yield is 97.1%.

Embodiment 2

[0043] Take 663g of 8 wt% Na 2 CO 3Stir the aqueous solution to cool down to below 20°C, start to slowly add 128g of α-acetyl-γ-butyrolactone dropwise, control the internal temperature at 18-22°C, part of the solid precipitates in the later stage of the reaction, add dropwise α-acetyl-γ-butyrolactone After the dropwise addition, stir and keep warm for 30 minutes, then add 200g of water to dissolve the precipitate, cool the system down to 10°C and slowly introduce chlorine gas, control the temperature of the reaction solution at 10-12°C, when the reaction solution finally turns milky white, the solution pH =5.8, end chlorine gas, nitrogen replacement, vacuum pumping for 10min, let stand and separate layers, the lower organic phase is α-chloro-α-acetyl-γ-butyrolactone, the gas phase content is 99.2%, and the molar yield is 96.8% .

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to the field of organic synthesis, and particularly discloses a method for preparing alpha-chloro-alpha-acetyl-gamma-butyrolactone. The preparation method comprises the followingsteps: (1) in the presence of a solvent, carrying out a salt forming reaction on alpha-acetyl-gamma-butyrolactone and at least one inorganic alkaline substance selected from NaOH, KOH, K2CO3 and Na2CO3 until a precipitate is generated, and then dissolving the precipitate to obtain a first solution; (2) carrying out a contact reaction on the first solution and chlorine to obtain a second solution;and (3) layering the second solution so as to obtain the alpha-chloro-alpha-acetyl-gamma-butyrolactone. The method has the advantages of simple operation, environmental protection, mild reaction conditions, and important practical significance.

Description

technical field [0001] The invention relates to the field of organic synthesis, in particular to a method for preparing α-chloro-α-acetyl-γ-butyrolactone. Background technique [0002] α-Chloro-α-acetyl-γ-butyrolactone is one of the main intermediates for the chemical synthesis of vitamin B1 (VB1), and its purity directly affects the quality of VB1. [0003] At present, commercially available α-chloro-α-acetyl-γ-butyrolactone products contain a small amount of polychloride, which obviously affects the product stability and is not easy to preserve. [0004] Therefore, providing a high-purity, stable α-chloro-α-acetyl-γ-butyrolactone standard reference substance has positive guiding significance for the research and development of high-quality VB1 products. [0005] In the traditional synthesis of α-chloro-α-acetyl-γ-butyrolactone process route, the raw material α-acetyl-γ-butyrolactone reacts with chlorinated reagents such as sulfonyl chloride at low temperature to form α-ch...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07D307/33
CPCC07D307/33
Inventor 俞诚陈义祥张平李全国万真
Owner 江西天新药业股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com