Process for preparation of alkynyl carboxylic acids

Patent metadata

Field	Value
Publication number	US-9302970-B2
Application number	US-201314374338-A
Country	US
Kind code	B2
Filing date	Jan 25, 2013
Priority date	Jan 25, 2012
Publication date	Apr 5, 2016
Grant date	Apr 5, 2016

Abstract

The invention provides a simple, efficient, environmentally friendly catalytic system for direct carboxylation reactions using CO 2 under mild conditions. A single step heterogeneous catalytic process for preparation of alkynyl carboxylic acids is disclosed.

First claim

We claim:

1. A process for preparation of an alkynyl carboxylic acid of formula:
R—C≡CO 2 H

wherein R is a monovalent substituent selected from the group consisting of straight or branched alkyl, straight or branched alkenyl, straight or branched alkenyloxy, straight or branched alkynyloxy, straight or branched alkenylthio, straight or branched alkynylthio, aryl, alkaryl, aralkenyl, aralkynyl, aryloxy, aralkoxy, cycloalkyl, heteroaryl, and a carbonyl, where each of these may be substituted with halo, hydroxyl, nitro, amino, cyano, carbonyl, alkoxy, carboxyl, ester, alkyl, alkenyl, alkynyl, thio, sulfonyl, sulfinyl, phenyl or heteroaryl by carboxylation of terminal alkyne with CO 2 , wherein said process comprises reacting a terminal alkyne of formula:
R—C≡C—H

wherein R is as above with carbon dioxide, in the presence of a heterogeneous copper(II) exchanged montmorillonite K-10 catalyst, cesium carbonate (Cs 2 CO 3 ) as a base and DMF as a solvent at temperature ranging between 50-60° C. for a period ranging between 12-16 h under a pressure of about 1 atm to obtain a compound of formula
R—C≡C—CO 2 H.

2. The process according to claim 1 , wherein the heterogeneous copper(II) exchanged montmorillonite K-10 catalyst is present in a range of 10-30 w/w %.

3. The process according to claim 1 , wherein the base is used in the range of 1-2 equivalents.

4. The process according to claim 1 , wherein yield of said alkynyl carboxylic acids is in the range of 70-94%.

5. The process according to claim 1 , wherein selectivity of catalyst for said alkynyl carboxylic acid is 100%.

Assignees

• Aher Ravindra Dattatray
• Gade Madhuri Hanumant
• Rekula Reddy Santhosh
• Karabal Pratibha Uttam
• Suryavanshi Gurunath Mallappa
• Sudalai Arumugam
• Council Scient Ind Res

Inventors

• Aher Ravindra Dattatray
• Gade Madhuri Hanumant
• Rekula Reddy Santhosh
• Karabal Pratibha Uttam
• Suryavanshi Gurunath Mallappa
• Sudalai Arumugam

Classifications

• C07C51/15 Primary

  by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis · CPC title

• C07C57/42

  having unsaturation outside the rings · CPC title

• C07C57/18

  with only carbon-to-carbon triple bonds as unsaturation · CPC title

• C07C59/64

  containing six-membered aromatic rings · CPC title