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

Synthesis method of 3-methoxyl-N, N-dimethylacrylamide

A dimethylpropionamide and synthesis method technology, applied in the synthesis of 3-methoxy-N,N-dimethylpropionamide, and in the field of synthesis of chemical material intermediates, can solve difficult processing, high energy consumption, The process is cumbersome and other problems, to achieve the effect of simple reaction, low energy consumption and simple operation

Active Publication Date: 2017-06-23
LINHAI LIANSHENG CHEM
View PDF10 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] For example, the Chinese patent (application number: 201380019269.8) discloses a method for the manufacture of β-alkoxypropionamides, in which β-alkoxy acrylates are reacted with amines to produce β-alkoxypropionamides , but this method uses β-alkoxy acrylates as raw materials and reacts with amines. After the reaction, the by-products need to be recovered, and the recovered by-products contain a large amount of amines, so it is difficult to handle, and the raw materials themselves are processed by acrylic acid. Obtained from esterification and methoxidation, the process is relatively cumbersome and the energy consumption is high

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
  • Synthesis method of 3-methoxyl-N, N-dimethylacrylamide
  • Synthesis method of 3-methoxyl-N, N-dimethylacrylamide
  • Synthesis method of 3-methoxyl-N, N-dimethylacrylamide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0037] The following are specific examples of the present invention to further describe the technical solutions of the present invention, but the present invention is not limited to these examples.

[0038] According to the parameters in Table 1 Examples 1-38 and Comparative Examples 3-20 and adopt the following method of the present invention to synthesize 3-methoxy-N,N-dimethylpropionamide:

[0039] S1. Synthesis of 3-methoxypropionitrile: Add acrylonitrile, anhydrous methanol and metal alkoxides to the reactor for alkoxylation first, then recover unreacted anhydrous methanol to obtain 3-methoxypropionitrile propionitrile;

[0040] Synthesis of S2, 3-methoxypropionic acid: adding acidic catalyst and water to 3-methoxypropionitrile in step S1, heating for hydrolysis reaction to obtain 3-methoxypropionic acid;

[0041] S3. Synthesis of 3-methoxy-N,N-dimethylpropionamide: Add 3-methoxypropanoic acid and dimethylamine into a closed reactor, heat up and react to obtain 3-methoxy...

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 a synthesis method of 3-methoxyl-N, N-dimethylacrylamide, and belongs to the technical field of chemical synthesis. The synthesis method comprises the following steps of adding 3-methoxypropionic acid and dimethylamine into a sealed reactor; raising the temperature to 80 to 150 DEG C; performing reaction to obtain 3-methoxyl-N, N-dimethylacrylamide, wherein the pressure in the sealed reactor is 0.1 to 10.0MPa. The 3-methoxypropionic acid is used as the raw materials to perform high-temperature dewatering with dimethylamine in a sealed reaction vessel; polyhydric alcohol and basic catalysts are not needed; the reaction is simple; the implementation is easy; the yield of a product is high; the purity is high; the high yield is realized; meanwhile, the pollution is little; the cost is low; the method conforms to the requirements of modern chemical green synthesis. Meanwhile, the 3-methoxypropionic acid uses low-price acrylonitrile as the starting raw materials; the acrylonitrile is subjected to alkoxylation to obtain methoxyl propionitrile; then, hydrolysis is performed. The operation is simple; the energy consumption is low.

Description

technical field [0001] The invention relates to a synthesis method of a chemical material intermediate, in particular to a synthesis method of 3-methoxy-N,N-dimethylpropionamide, which belongs to the technical field of chemical synthesis. Background technique [0002] 3-methoxy-N,N-dimethylpropionamide (structural formula shown in formula I), is a colorless and transparent solvent, has amide groups and alkyl groups, can be mixed with various solvents, can Highly soluble polymer polyamide; it has the characteristics of high solubility, high permeability, high fluidity, low viscosity, low surface tension, etc., and is not irritating to the skin, safe and environmentally friendly, and can be a good substitute for the traditional solvent N-formazan Pyrrolidone is widely used in electronics, medicine, pesticides, pigments, cleaning agents, insulating materials and other industries. Nowadays, in the increasingly competitive safe solvent market, in addition to solubility, high vol...

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): C07C231/02C07C233/05
CPCC07C51/08C07C231/02C07C253/30C07C233/05C07C255/13C07C59/125
Inventor 黄卫国强永康姚素
Owner LINHAI LIANSHENG CHEM
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