Issue 36, 2022

Direct photochemical route to azoxybenzenes via nitroarene homocoupling

Abstract

We report on a direct photochemical method for the one-pot, catalyst- and additive-free synthesis of azoxybenzene and substituted azoxy derivatives from nitrobenzene building blocks. This reaction is conducted at room temperature and under air, and can be applied to substrates with a wide range of substituents. Yields of products derived from para- and meta-substituted nitrobenzenes are typically good, while sterically encumbered ortho-substituted substrates are not as fruitful. Photochemical Wallach rearrangement of generated azoxybenzenes to ortho-hydroxyazoxybenzenes was observed in some cases, most markedly in selected ortho-halogenated nitrobenzenes. Overall, this method provides an efficient, green pathway to highly value-added azoxybenzene products.

Graphical abstract: Direct photochemical route to azoxybenzenes via nitroarene homocoupling

Supplementary files

Article information

Article type
Paper
Submitted
12 Jul 2022
Accepted
02 Sep 2022
First published
02 Sep 2022

Org. Biomol. Chem., 2022,20, 7332-7337

Direct photochemical route to azoxybenzenes via nitroarene homocoupling

A. Yaghoubian, G. K. Hodgson, M. J. Adler and S. Impellizzeri, Org. Biomol. Chem., 2022, 20, 7332 DOI: 10.1039/D2OB01247B

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