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

Method for preparing cyclic carbonate employing catalysis of carbon dioxide and epoxide with haloid

A technology of cyclic carbonates and epoxides, which is applied in the field of organic synthesis catalysis, can solve problems such as complexity, cost, and poor reaction effect, achieve mild reaction conditions and reduce production costs

Inactive Publication Date: 2015-06-24
DALIAN UNIV OF TECH
View PDF4 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Various methods for CO have been reported in the prior art 2 The catalytic system for synthesizing cyclic carbonates with epoxides, in the patent application number 201110442303.5 applied by the Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, is a double-quaternized ionic liquid grafted with silica gel as a catalyst; Chengdu Organic, Chinese Academy of Sciences In the patent application number 201110062979.1 applied by Chemical Co., Ltd., the metal molybdate is used as the catalyst, and the organic quaternary ammonium salt or alkali metal halide is used as the promoter; there are other metal oxides, metal complexes and organic and inorganic Hybrid catalysts, etc. (J. Am. Chem. Soc., 2013, 135, 18497-18501; J. Am. Chem. Soc. 2013, 135, 11996?2003), but these catalyst systems are relatively complex or expensive
[0005] Inexpensive and readily available halogen-anion salts have also been used to catalyze CO 2 Synthesis of cyclic carbonates with epoxides, but under solvent-free conditions it catalyzes CO 2 Poor reaction with epoxides to synthesize cyclic carbonates (Tetrahedron Lett., 2008, 49, 3588-3591)

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

Embodiment 1

[0014] Add ethanol (71.5 mmol), ethylene oxide (14.3 mmol), and potassium iodide (1.43 mmol) into a 75 mL autoclave, and then introduce carbon dioxide to make the system pressure reach 0.5 MPa, react at 120 °C for 1 hour, and pass through the gas phase Chromatographic internal standard method quantitative analysis to obtain the productive rate of product ethylene carbonate 99.5%.

Embodiment 2

[0016] Add ethanol (71.5 mmol), propylene oxide (14.3 mmol), and potassium iodide (1.43 mmol) into a 75 mL autoclave, and then introduce carbon dioxide to make the system pressure reach 0.5 MPa, react at 120 °C for 1 hour, and pass through gas chromatography Quantitative analysis by the internal standard method obtained a yield of 93.6% of the product propylene carbonate.

Embodiment 3

[0018] Add ethanol (71.5 mmol), propylene oxide (14.3 mmol), and tetrabutylammonium iodide (1.43 mmol) into a 75 mL autoclave, then feed carbon dioxide to make the system pressure reach 0.5 MPa, and react 1 at 120 °C Hour, obtain the productive rate 88.0% of product propylene carbonate by gas chromatography internal standard method quantitative analysis.

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 preparing cyclic carbonate employing catalysis of carbon dioxide and epoxide with haloid, and belongs to the field of organic synthesis catalysis. According to the method, with haloid employing halogen serving as an anion as a catalyst, cycloaddition reaction employing carbon dioxide and epoxide as raw materials is catalyzed by adopting haloid which uses halogen serving as an anion as a catalyst. The catalyst is cheap and available; the production cost is reduced; the method is simple to operate in synthesis of the cyclic carbonate; the catalyst is cheap and available; the reaction condition is mild; the lowest initial reaction pressure can be as low as 0.25MPa; the catalyst is high in activity; the yield of ethylene carbonate is 99.5% under the optimal reaction condition; and with relatively environment-friendly alcohols as a solvent, the method conforms to the idea of green chemistry, and is an excellent system for preparing the cyclic carbonate.

Description

technical field [0001] The invention relates to a method for preparing cyclic carbonates by catalyzing carbon dioxide and epoxides with halide salts, which belongs to the field of organic synthesis catalysis. Background technique [0002] With the intensification of the "greenhouse effect", the effective use of inert carbon dioxide to achieve green chemical reactions has become a research hotspot in recent years (J. Am. Chem. Soc. 2014, 136, 6142-6147; J. Am. Chem. Soc . 2013, 135, 11996-12003). [0003] Cyclic carbonates are a class of widely used chemicals and solvents with high boiling point and high polarity. They have been used in many fields such as organic synthesis intermediates, battery electrolytes, and metal extractants (Green Chem. ). [0004] CO 2 The reaction of cycloaddition with epoxide to prepare cyclic carbonate has 100% atom economy, which is a typical atom economy reaction and conforms to the development direction of green chemistry. Various methods f...

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 Applications(China)
IPC IPC(8): C07D317/36C07D317/38
CPCC07D317/36C07D317/38
Inventor 刘春张绍科
Owner DALIAN UNIV OF TECH
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