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

Method for catalytically synthesizing mono-butyl itaconate at high selectivity

A technology for synthesizing monobutyl itaconic acid and selectivity is applied in chemical instruments and methods, preparation of organic compounds, preparation of carboxylic acid esters, etc. The effect of short reaction time and high catalytic efficiency

Inactive Publication Date: 2015-03-18
SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI
View PDF7 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there is no report on the application of common solid acid catalysts such as zeolites in this type of reaction.

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
  • Method for catalytically synthesizing mono-butyl itaconate at high selectivity
  • Method for catalytically synthesizing mono-butyl itaconate at high selectivity
  • Method for catalytically synthesizing mono-butyl itaconate at high selectivity

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] 13g of itaconic acid and 22.2g of n-butanol were weighed and heated and stirred in a three-necked flask, and the reaction temperature was controlled at 105°C. After stirring evenly, 0.26g of nanometer ZSM-5 clusters were added as a catalyst, and the reaction was carried out for 9 hours. Monobutyl itaconate was separated by centrifugation and crystallized at low temperature at 10°C as the initial product. During the reaction, it was quantified by GC-MS, and n-dodecane was used as internal standard.

[0039] figure 1 It can be seen that the nanocrystalline clusters are small crystal grains of 30-80 nm in a certain orientation to form irregular spheres with a size of about 500 nm. The corresponding TEM images and electron diffraction patterns confirm that the arrangement of small crystal grains has a certain orientation, which is not a traditional polycrystalline structure.

[0040] see image 3 , in the present embodiment, the nanometer ZSM-5 cluster is used as a cataly...

Embodiment 2

[0042] The catalyst is large particle ZSM-5 zeolite, see figure 2 , the particle size is about 1500nm, and the specific surface area is 370m 2 g -1 , the pore volume is 0.15cm 3 g -1 . According to the method of Example 1, the corresponding catalytic performance test and cycle test were carried out.

[0043] see Figure 4 , the traditional large zeolite in the butyl esterification reaction of itaconic acid, the generation rate of 6h monobutyl ester is 70%, the generation rate of dibutyl ester is 11%, and the selectivity of monobutyl ester is 86%. After the esterification of the carboxyl group at the β position of itaconic acid is completed, the diffusion distance from the pores is long, so part of the monoester continues to be esterified to form a diester, which reduces the reaction selectivity. On the other hand, the higher reactivity of nanocrystalline clusters was confirmed by the total ester yield of 81% for conventional zeolites relative to nanoclusters (93%).

Embodiment 3～5

[0045] The nano-ZSM-5 cluster catalyst in Example 1 was separated from the reaction system by centrifugation at 10000r / min for 10min, dried in an oven at 100°C for 2h, and then the mass ratio of the catalyst to itaconic acid was 2%, and the cycle test was carried out 3 times to verify The deactivation performance of the catalyst, the reaction temperature is about 105°C, and the catalytic reaction time is 6h.

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

PropertyMeasurementUnit
particle diameteraaaaaaaaaa
Login to View More

Abstract

The invention relates to a method for catalytically synthesizing mono-butyl itaconate at high selectivity. The method comprises the following step: with ZSM-5 zeolite as a catalyst, selectively and catalytically synthesizing mono-butyl itaconate through an esterification reaction between itaconic acid and n-butyl alcohol. According to the method, the mono-butyl itaconate is selectively synthesized by using a solid acid catalyst limited by a molecular channel, the excessive n-butyl alcohol serves as a water-carrying agent, and the method is low in catalytic reaction temperature, short in catalytic reaction time and high in catalytic efficiency and is suitable for industrial application. The catalyst has high catalytic activity in selective synthesis of mono-butyl itaconate. The solid acid catalyst is easily separated from the reaction system, is slight in pollution and has high recyclability.

Description

technical field [0001] The invention belongs to the field of inorganic catalysis and organic synthesis. It specifically relates to the use of nanometer ZSM-5 zeolite as a catalyst, which can selectively synthesize monobutyl itaconate with high yield in the catalytic reaction of itaconic acid and n-butanol. Background technique [0002] Itaconic acid, also known as methylene succinic acid, is an important active monomer in the field of polymer chemical industry because it contains a C=C unsaturated double bond. It can undergo esterification reaction with alcohol to form monoester or diester, in which the carboxyl group at the α position has a conjugated double bond, and its activity is lower than that of the carboxyl group at the β position, so the monoester is mainly esterified with the carboxyl group at the β position, such as itaconic acid monobutyl ester. At present, itaconate esters reported in the literature mainly include methyl itaconate, ethyl itaconate, propyl ita...

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): C07C69/593C07C67/08
Inventor 朱颜华子乐宋禹奠周晓霞龚云王立军施剑林
Owner SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI
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