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

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]BF(4) as a photoredox catalyst and molecular oxygen as a green oxidant under visible light was developed. This photo...

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Detalles Bibliográficos
Autores principales: Neerathilingam, Nalladhambi, Anandhan, Ramasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984950/
https://www.ncbi.nlm.nih.gov/pubmed/35424823
http://dx.doi.org/10.1039/d2ra00585a
Descripción
Sumario: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]BF(4) 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]BF(4) based on a Stern–Volmer plot, which led to the proposed mechanism of this reaction.