Issue 42, 2021

Copper-catalysed low-temperature water–gas shift reaction for selective deuteration of aryl halides

Abstract

The introduction of deuterium atoms into organic compounds is of importance for basic chemistry, material sciences, and the development of drugs in the pharmaceutical industry, specifically for identification and quantification of metabolites. Hence, methodologies for the synthesis of selectively labelled compounds continue to be a major area of interest for many scientists. Herein, we present a practical and stable heterogeneous copper catalyst, which permits for dehalogenative deuteration via water–gas shift reaction at comparably low temperature. This novel approach allows deuteration of diverse (hetero)aryl halides with good functional group tolerance, and no reduction of the aromatic rings or other easily reducible formyl and cyano groups. Multi-gram experiments show the potential of this method in organic synthesis and medicinal chemistry.

Graphical abstract: Copper-catalysed low-temperature water–gas shift reaction for selective deuteration of aryl halides

Supplementary files

Article information

Article type
Edge Article
Submitted
04 Aug. 2021
Accepted
17 Sept. 2021
First published
17 Sept. 2021
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2021,12, 14033-14038

Copper-catalysed low-temperature water–gas shift reaction for selective deuteration of aryl halides

W. Li, R. Qu, W. Liu, F. Bourriquen, S. Bartling, N. Rockstroh, K. Junge and M. Beller, Chem. Sci., 2021, 12, 14033 DOI: 10.1039/D1SC04259A

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