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

A kind of synthetic method of 5-methyl-2-pyrrolidone or its derivatives

A technology of pyrrolidone and a synthesis method, applied in the field of organic catalysis synthesis, can solve the problems of difficulty in product separation and purification, solvent volatilization and recovery, low product selectivity, etc., and achieves the effects of being beneficial to separation, avoiding side reactions and simple reaction system

Active Publication Date: 2021-07-09
XIAMEN UNIV
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The purpose of the present invention is to overcome the deficiencies of the prior art, and provides a synthetic method of 5-methyl-2-pyrrolidone or its derivatives, which solves the problem of high hydrogen pressure and a large amount of organic matter caused by the external hydrogen source in the above-mentioned background technology. The problem of solvent volatilization and recovery caused by solvent use also solves the problems of low product selectivity and difficulty in product separation and purification

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
  • A kind of synthetic method of 5-methyl-2-pyrrolidone or its derivatives
  • A kind of synthetic method of 5-methyl-2-pyrrolidone or its derivatives
  • A kind of synthetic method of 5-methyl-2-pyrrolidone or its derivatives

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1～6

[0031] Take 0.05mol of levulinic acid, methyl levulinate, ethyl levulinate, propyl levulinate, butyl levulinate, amyl levulinate respectively, and put them in high pressure reaction with equimolar urea and formic acid In the still, add 0.174g ruthenium carbon catalyst and mix evenly, seal the reaction kettle, heat to 130°C under magnetic stirring and keep for 6h respectively, finish the reaction and cool to room temperature and filter to recover the catalyst. GC-MS (Shimadzu) and GC (Agilent) were used for qualitative and quantitative detection, and the detection results are listed in Table 1 with serial numbers 1-6.

Embodiment 7～16

[0033] Take 0.1mol formamide, acetamide, propionamide, benzamide, phenylacetamide, N-methylformamide, N-methylacetamide, N-methylpropionamide, N-methylbenzamide respectively , N-methylphenylacetamide, put 0.05mol ethyl levulinate and 0.1mol formic acid in a high-pressure reactor, then add 0.29g platinum carbon catalyst and mix evenly, seal the reactor, heat to 100°C under magnetic stirring and Respectively keep 24h, finish the reaction and cool to room temperature and filter to recover the catalyst. GC-MS (Shimadzu) and GC (Agilent) were used for qualitative and quantitative detection, and the detection results are listed in Table 1 with serial numbers 7-16.

Embodiment 17～25

[0035] Take 0.05mol levulinic acid, 0.06mol formic acid, and 0.075mol urea in a high-pressure reactor, and then add 0.58g of rhodium carbon, palladium carbon, ruthenium carbon / copper oxide, platinum carbon / copper oxide, rhodium carbon / copper oxide , palladium carbon / copper oxide, platinum / molybdenum oxide, platinum / titanium dioxide, and platinum / zirconia catalysts were mixed evenly, and the reaction vessel was sealed, heated to 80°C under magnetic stirring and kept for 4 hours respectively. After the reaction was completed, the reaction was cooled to room temperature and the catalyst was recovered by filtration. GC-MS (Shimadzu) and GC (Agilent) were used for qualitative and quantitative detection, and the detection results are listed in Table 1 with serial numbers 17-25.

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 method for synthesizing 5-methyl-2-pyrrolidone or derivatives thereof, which comprises the following steps: fully mixing levulinic acid (ester) with urea or amide and formic acid, and adding them into a high-pressure reaction kettle together with a catalyst After the reaction, the target product 5-methyl-2-pyrrolidone and its derivatives are obtained; after the reaction is completed, the catalyst is recovered by filtration, washed and dried, and reused. The method of the invention can realize high-efficiency conversion of levulinic acid (ester) in a solvent-free system, the cheap and environment-friendly urea or amide is used as the N source, and the biomass-based formic acid is used as the H source, and has good economy.

Description

technical field [0001] The invention belongs to the technical field of organic catalytic synthesis, and in particular relates to a synthesis method of 5-methyl-2-pyrrolidone or derivatives thereof. Background technique [0002] Pyrrolidone compounds are an important class of industrial chemicals and fine intermediates. In addition to being widely used as solvents, they can also be used in petrochemical processing, polymer synthesis, agricultural and pharmaceutical intermediates, surfactants for inks and coatings, and industrial cleaning agents. and dispersants, as well as in the manufacture of graphene and lithium-ion batteries. However, some pyrrolidone compounds, such as N-methylpyrrolidone, inevitably have toxicity and high cost in the production process, as well as increasingly stringent regulations, forcing people to seek safer and cheaper pyrrolidone compounds to replace N-methylpyrrolidone Used as a solvent. Among them, 5-methyl-2-pyrrolidone and its derivatives hav...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C07D207/267
CPCC07D207/267Y02P20/584
Inventor 林鹿唐兴孙勇曾宪海雷廷宙曹雪娟
Owner XIAMEN UNIV
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