Issue 82, 2016, Issue in Progress

A palladium–bisoxazoline supported catalyst for selective synthesis of aryl esters and aryl amides via carbonylative coupling reactions

Abstract

The catalytic synthesis of aryl esters and amides has been successfully achieved in the presence of the efficient palladium–bisoxazoline supported on Merrifield's resin (Pd–BOX-M). The palladium heterogeneous catalyst was prepared and characterized using various spectroscopic techniques. A bisoxazoline ligand having a suitable functional group (BOX-OH) was first synthesized, characterized, chemically supported on Merrifield's resin, and finally coordinated to palladium(II) chloride. The catalytic activity and the recycling ability of the new palladium supported catalyst have been investigated in the alkoxycarbonylation and aminocarbonylation of various aryl iodides using different alkyl and aromatic alcohols and amines as nucleophiles. The palladium heterogeneous catalyst demonstrated excellent catalytic activity and very high recycling ability in the above two carbonylation reactions. The palladium heterogeneous catalysts showed an excellent stability under carbon monoxide and under the experimental conditions.

Graphical abstract: A palladium–bisoxazoline supported catalyst for selective synthesis of aryl esters and aryl amides via carbonylative coupling reactions

Supplementary files

Article information

Article type
Paper
Submitted
15 Jun 2016
Accepted
15 Aug 2016
First published
15 Aug 2016

RSC Adv., 2016,6, 78826-78837

A palladium–bisoxazoline supported catalyst for selective synthesis of aryl esters and aryl amides via carbonylative coupling reactions

M. B. Ibrahim, R. Suleiman, M. Fettouhi and B. El Ali, RSC Adv., 2016, 6, 78826 DOI: 10.1039/C6RA15506E

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