Issue 57, 2023

Carboamination and olefination: ortho C–H functionalization of phenoxyacetamide

Abstract

Herein, we have demonstrated a rhodium-catalyzed carboamination of olefin with the double bond intact. For the first time, deacylative carboamination of the maleimide has been achieved wherein phenoxyacetamide has behaved as the aminating source. In addition to carboamination, we have also disclosed the C–H olefination protocol where the maleimide group has been installed successfully in the ortho-position of phenoxyacetamide. In this protocol, phenoxyacetamide behaved as a traceless directing group with the in situ release of acetamide. The base-assisted E2-elimination is the key to the success of the olefination reaction.

Graphical abstract: Carboamination and olefination: ortho C–H functionalization of phenoxyacetamide

Supplementary files

Article information

Article type
Communication
Submitted
05 mai 2023
Accepted
15 jun 2023
First published
15 jun 2023

Chem. Commun., 2023,59, 8818-8821

Carboamination and olefination: ortho C–H functionalization of phenoxyacetamide

T. Nanda, S. K. Dhal, G. K. Das Adhikari, N. Prusty and P. C. Ravikumar, Chem. Commun., 2023, 59, 8818 DOI: 10.1039/D3CC02202A

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