Process for the selective oxidation of organic compounds

A technology of organic compounds and oxides, applied in organic chemical methods, organic chemistry, organic compound/hydride/coordination complex catalysts, etc., can solve water sensitivity and other problems

Inactive Publication Date: 2001-01-03
DU PONT PHARMA CO
View PDF1 Cites 16 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Catalytic oxidation processes are important processes for many commercial chemicals, for example many commercial processes for the epoxidation of olefins have been disclosed in the art, one such process involves certain soluble transition metal compounds (e.g. molybdenum, tungsten , naphthenates of vanadium) in the presence of organic hydroperoxides and olefins, some of the disadvantages of this process include the simultaneous production of alcohol from the hydroperoxide, the recovery of soluble metal catalysts, and the sensitivity of the reaction to water.

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

[0061] The epoxidation of embodiment 1 1-octene

[0062] Add 3% hydrogen peroxide aqueous solution (1.09g) and 1-octene (2.05g) to catalyst B (50mg), stir the mixture at room temperature, after 24 hours, GC analysis shows that 1,2 - Epoxyoctane (18% yield calculated as peroxide).

Embodiment 2

[0063] Example 2 The epoxidation of 1-octene

[0064] Add 3% aqueous hydrogen peroxide solution (1.03g) and 1-octene (2.14g) to catalyst B2 (98mg), stir the mixture at room temperature, and after 24 hours, GC analysis shows that 1,2 - Epoxyoctane (yield 11% calculated as peroxide).

Embodiment 3

[0065] Example 3 Epoxidation of cis-cyclooctene

[0066] Add 10% hydrogen peroxide aqueous solution (1.05g) and cis-cyclooctene (2.44g) in catalyst B2 (91mg), stir the mixture at room temperature, after 24 hours, GC analysis shows that there is cyclooctene oxide (in the form of peroxide The calculated yield was 33%).

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

A process for oxidizing organic compounds is disclosed. Hydrogen peroxide is used to oxidize an oxidizable organic substrate in the presence of a silica-modified titania/silica-containing catalyst. A method for preparing a catalyst using a copolymer of diethoxysilane and ethyl titanate is also disclosed.

Description

field of invention [0001] The present invention relates generally to methods of oxidizing organic compounds, and more particularly to methods of oxidizing oxidizable organics using hydrogen peroxide in the presence of silica-modified titania / silica-containing catalysts, and the use of di A method for preparing a catalyst from a copolymer of ethoxysilane and ethyl titanate. background of the invention [0002] Catalytic oxidation processes are important processes for many commercial chemicals, for example many commercial processes for the epoxidation of olefins have been disclosed in the art, one such process involves certain soluble transition metal compounds (e.g. molybdenum, tungsten , naphthenate of vanadium) in the presence of organic hydroperoxides and olefins, some of the disadvantages of this process include the simultaneous production of alcohol from the hydroperoxide, the recovery of soluble metal catalysts, and the sensitivity of the reaction to water. [0003] He...

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): A61K51/12A61N5/10B01J31/12C07B33/00C07B41/00C07B61/00C07D301/12C07D303/04
CPCA61N5/1027A61N2005/1024C07D301/12C07B41/00A61K51/1282C07D303/04A61N2005/1019B01J29/89
Inventor P·R·辛格G·P·特肖小J·N·文茨K·R·奥莱瓦恩
Owner DU PONT PHARMA CO
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