Preparation method of 4-acetoxyl-2-methyl-2-butylenoic aldehyde

A technology of acetoxy and crotonaldehyde, applied in the field of preparation of 4-acetoxy-2-methyl-2-butenal, which can solve the problem of high equipment requirements and achieve good reaction selectivity and high yield , the effect of less by-products

Active Publication Date: 2010-06-09
SHANGYU NHU BIOCHEM IND
View PDF5 Cites 24 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0013] The French high temperature and high pressure noble metal cat

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of 4-acetoxyl-2-methyl-2-butylenoic aldehyde
  • Preparation method of 4-acetoxyl-2-methyl-2-butylenoic aldehyde
  • Preparation method of 4-acetoxyl-2-methyl-2-butylenoic aldehyde

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0039] A. Preparation of chloroester (III)

[0040] Add 61g of acetic anhydride to a 250ml four-neck flask, add 3g of ion exchange resin loaded with periodic acid at room temperature, stir for about 15min, raise the temperature to 50°C, start adding 40g of 2-chloroethanol dropwise, finish the dripping in about 30min, and keep warm for the reaction 5h. After GC analysis, no 2-chloroethanol remains, and the temperature is lowered to about 10°C to filter out the catalyst-loaded periodic acid ion exchange resin, add 100ml of dichloromethane to the filtrate and dropwise add 10% sodium hydroxide solution to adjust the pH of the aqueous phase 6-7, the organic phase was separated, and the aqueous phase was extracted with dichloromethane and incorporated into the organic phase. The organic phase was washed once with 150 ml of saturated brine, and then dichloromethane was recovered under reduced pressure to obtain 60 g of chloroester (III), which was analyzed by GC with a content of 92...

Embodiment 2

[0049] A. Preparation of bromoester (III)

[0050] Add 61g of acetic anhydride to a 250ml four-neck flask, add 3g of ion exchange resin loaded with periodic acid at room temperature, stir for about 15min, heat up to 50°C, start to add 62g of 2-bromoethanol dropwise, finish dropping in about 30min, and keep warm for the reaction 5h. After GC analysis, there is no 2-bromoethanol residue, and the temperature is lowered to about 10°C to filter out the catalyst-loaded periodate ion exchange resin, add 100ml of dichloromethane to the filtrate and add 10% sodium hydroxide solution dropwise to adjust the pH of the water phase 6-7, the organic phase was separated, and the aqueous phase was extracted with dichloromethane and incorporated into the organic phase. The organic phase was washed once with 150 ml of saturated brine, and then dichloromethane was recovered under reduced pressure to obtain 82.5 g of bromoester (III). According to GC analysis, the content was 91.8%, and the yield...

Embodiment 3

[0059] A. prepare chloroester (III) with the same method of embodiment 1

[0060] B. Preparation of Phosphonate (IV)

[0061]Add 75g of triethyl phosphite into a 250ml four-neck flask, raise the temperature to 140°C, start to add 50g of chloroester (III) (content: 92.5%) dropwise, and finish dropping in about 45 minutes. temperature rise

[0062] Take a sample after holding the reaction for 1 hour at 150°C, and analyze by GC that the residual chloroester is less than 1%. Cool down to 70°C, remove the first part by depressurizing with an oil pump, until the temperature rises to 100°C and no leakage occurs, and finally 85.6g of phosphonate is obtained , GC test content 92.7%, yield 93.8%.

[0063] C. Preparation of five-carbon aldehyde acetal (V)

[0064] Add phosphonate (IV) 48g (content 92.7%) and 100ml toluene in a 250ml three-necked flask, stir for 5min, add 24.5g (content 96%) 1,1-dimethoxyacetone, under normal temperature (20-30 ℃) Add 14g of sodium hydroxide, and keep...

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 discloses a preparation method of 4-acetoxyl-2-methyl-2-butylenoic aldehyde. In the traditional method, the yield is lower, the waste water amount is larger, and the requirements on equipment are higher. The preparation method comprises the following steps of: reacting 2-halogenated ethanol as a raw material with an acylating agent to obtain halogenated ester; then preparing phosphonate ester through the Arbuzov reaction between the halogenated ester and triethyl phosphite; preparing glutaraldehyde acetal through the Wittig-Horner reaction between the phosphonate ester and 1,1-dimethoxy acetone under the action of alkaline, and carrying out deprotection on the glutaraldehyde acetal under the acidic condition to obtain glutaraldehyde, namely, the 4-acetoxyl-2-methyl-2-butylenoic aldehyde. The invention has less three waste generation, good reaction selectivity, less by-products and higher yield.

Description

technical field [0001] The invention relates to a preparation method of 4-acetoxy-2-methyl-2-butenal. Background technique [0002] 4-acetoxy-2-methyl-2-butenal (hereinafter referred to as five-carbon aldehyde), which is a key intermediate for the synthesis of vitamin A, the current synthetic methods mainly include dimethoxyacetone method, ethylene oxide Alkane method, isoprene method and butylene glycol method. [0003] US5453547 and US4301048 have described the method that dimethoxyacetone method prepares pentacarbon aldehyde, and its reaction process is as follows: [0004] , [0005] This method uses alkynylation and hydrogenation, has high operation requirements, and the yield of copper-catalyzed isomerization is low. US4873362 has described the method for each five carbon aldehydes of oxirane legal system, and its reaction process is as follows: [0006] , [0007] In this method, ethylene oxide is a high-risk raw material, and the intermediate acetoxyacetalde...

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): C07C69/145C07C67/297
Inventor 张明锋王正江黄国东周贵阳盛晓军车煜华
Owner SHANGYU NHU BIOCHEM IND
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap