Issue 14, 2022, Issue in Progress

Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light

Abstract

An efficient synthesis of imides using metal-free photoredox-catalyzed direct α-oxygenation of N,N′-disubstituted anilines in the presence of 9-mesityl-10-methylacridinium [Acr+-Mes]BF4 as a photoredox catalyst and molecular oxygen as a green oxidant under visible light was developed. This photochemical approach offered operational simplicity, high atom economy with a low E-factor, and functional group tolerance under mild reaction conditions. Control and quenching experiments confirmed the occurrence of a radical pathway and superoxide radical anion α-oxygenation reactions, and also provided strong evidence for the reductive quenching of [Acr+-Mes]BF4 based on a Stern–Volmer plot, which led to the proposed mechanism of this reaction.

Graphical abstract: Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light

Supplementary files

Article information

Article type
Paper
Submitted
27 Jan 2022
Accepted
12 Feb 2022
First published
15 Mar 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 8368-8373

Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light

N. Neerathilingam and R. Anandhan, RSC Adv., 2022, 12, 8368 DOI: 10.1039/D2RA00585A

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