Direct catalytic partial oxidation of allyl ether

Patent metadata

Field	Value
Publication number	US-10138197-B2
Application number	US-201815904581-A
Country	US
Kind code	B2
Filing date	Feb 26, 2018
Priority date	Mar 13, 2017
Publication date	Nov 27, 2018
Grant date	Nov 27, 2018

Abstract

This disclosure describes a new route to acrylate esters via direct catalytic partial oxidation of allyl ether using heterogeneous manganese oxide catalysts. The method involves forming allyl acrylate by contacting allyl ether, where the allyl ether is in solution with a solvent, with one or more oxidants in the presence of a mesoporous manganese oxide (MnOx) catalyst. Oxygen or peroxide can be used as the oxidant. The yield of and selectivity for acrylate ester can be very high, and process efficiency is improved over current processes.

First claim

The invention claimed is:

1. A process for forming allyl acrylate, comprising contacting allyl ether with a solvent, wherein the solvent is selected from acetonitrile, chloroform, dichloromethane, N,N-dimethylformamide, N,N-dimethyl acetamide, dimethyl sulfoxide, or dimethylcarbonate, and with an oxidant, wherein the oxidant is selected from oxygen, oxygen-containing gases, peroxides, and mixtures thereof in the presence of a mesoporous manganese oxide (MnOx) catalyst.

2. The process of claim 1 , wherein the solution further comprises trichloromethyl cyanide and/or N-hydroxyphthalimide.

3. The process of claim 1 , wherein the mesoporous manganese oxide catalyst is promoted with promoter cations of Group I or Group II metals.

4. The process of claim 3 , wherein the promoter ions are selected from the group consisting of Li, Na, K, Rb, Cs, Ca, Sr and Ba ions, and combinations thereof.

5. The process of claim 4 , wherein the promoter ions are Li ions.

6. The process of claim 1 , wherein the mole ratio of solvent to allyl ether is from 47:1 to 200:1.

7. The process of claim 6 , wherein the mole ratio of solvent to allyl ether is from 94:1 to 190:1.

8. The process of claim 1 , wherein the conversion of allyl ether to allyl acrylate is from 10% to 92%.

9. The process of claim 1 , wherein the selectivity for allyl acrylate is from 40% to 100%.

10. The process of claim 1 , which is conducted at a temperature of from 10° C. to 110° C.

11. The process of claim 1 , which is conducted at a temperature of from 40° C. to 90° C.

12. The process of claim 1 , which is conducted at a temperature of from 45° C. to 80° C.

13. The process of claim 1 , which is conducted at a pressure of from 0.1 atm to 3 atm.

14. The process of claim 1 , which is conducted over a period from 0.1 hour to 16 hours.

15. The process of claim 1 , which is conducted over a period from 1 hour to 10 hours.

Assignees

• Exxonmobil Res & Eng Co

Inventors

• Nandi Partha
• Suib Steven L
• Shaffer Timothy D

Classifications

• C07C51/285 Primary

  with peroxy-compounds · CPC title

• C07C51/25

  of unsaturated compounds containing no six-membered aromatic ring · CPC title

• B01J23/34 Primary

  Manganese · CPC title

• B01J23/04

  Alkali metals · CPC title

• C07C67/39

  by oxidation of groups which are precursors for the acid moiety of the ester · CPC title