Issue 15, 2018

Copper-catalyzed oxidative coupling of arylboronic acids with aryl carboxylic acids: Cu3(BTC)2 MOF as a sustainable catalyst to access aryl esters

Abstract

A convenient and sustainable method is demonstrated for the oxidative coupling of arylboronic acids with aryl carboxylic acids via C–O cross-coupling reaction catalyzed by the unsaturated coordination sites of copper present in the Cu3(BTC)2 MOF. Using air as an environment-friendly oxidant, the as-prepared Cu3(BTC)2 was employed in a MOF-based catalysis reaction with high efficiency and high chemoselectivity without the use of any external oxidants, ligands or additives. The present methodology avoids stoichiometric reagents and special reaction conditions, and shows excellent functional group tolerance with decent to excellent yields of aryl esters. The catalyst was found to exhibit high stability and reusability, without loss in activity even after several cycles, which was evident from the FT-IR, PXRD, and SEM characterizations of the reused catalyst.

Graphical abstract: Copper-catalyzed oxidative coupling of arylboronic acids with aryl carboxylic acids: Cu3(BTC)2 MOF as a sustainable catalyst to access aryl esters

Supplementary files

Article information

Article type
Research Article
Submitted
26 May 2018
Accepted
13 Jun 2018
First published
13 Jun 2018

Org. Chem. Front., 2018,5, 2322-2331

Copper-catalyzed oxidative coupling of arylboronic acids with aryl carboxylic acids: Cu3(BTC)2 MOF as a sustainable catalyst to access aryl esters

N. Devarajan and P. Suresh, Org. Chem. Front., 2018, 5, 2322 DOI: 10.1039/C8QO00519B

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