Issue 8, 2015

A novel nickel-catalyzed synthesis of thioesters, esters and amides from aryl iodides in the presence of chromium hexacarbonyl

Abstract

This study describes our findings on a novel and cheap NiCl2 catalytic system under ligand-free conditions for the efficient thiocarbonylation, alkoxycarbonylation and amidocarbonylation reactions of aryl iodides in the presence of Cr(CO)6 as the solid source of carbon monoxide under air. A variety of aryl iodides tolerated the reaction conditions and structurally different thiols, alcohols and amines were used efficiently. The corresponding thioesters, esters and amides were obtained in good to excellent yield at atmospheric pressure under mild reaction conditions.

Graphical abstract: A novel nickel-catalyzed synthesis of thioesters, esters and amides from aryl iodides in the presence of chromium hexacarbonyl

Supplementary files

Article information

Article type
Paper
Submitted
16 Mar 2015
Accepted
11 Jun 2015
First published
12 Jun 2015

New J. Chem., 2015,39, 6445-6452

A novel nickel-catalyzed synthesis of thioesters, esters and amides from aryl iodides in the presence of chromium hexacarbonyl

N. Iranpoor, H. Firouzabadi, E. Etemadi-Davan, A. Nematollahi and H. R. Firouzi, New J. Chem., 2015, 39, 6445 DOI: 10.1039/C5NJ00655D

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