Issue 59, 2019

Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols

Abstract

A catalyst-free method for the hydroxylation of arylboronic acids to form the corresponding phenols with sodium perborate as the oxidant was developed using water as the solvent. Under the reaction conditions, the yield of phenol reached 92% at only 5 min. Moreover, the reaction could be conducted without a catalyst under the solvent-free condition, the efficiency of which was as high as that of a liquid-phase reaction. Using a microcalorimeter, the reaction was found to be an exothermic reaction. The reaction mechanism was investigated and understood via DFT calculations, which revealed that it was a nucleophilic reaction.

Graphical abstract: Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols

Supplementary files

Article information

Article type
Paper
Submitted
08 Sep 2019
Accepted
11 Oct 2019
First published
25 Oct 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 34529-34534

Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols

X. Yang, X. Jiang, W. Wang, Q. Yang, Y. Ma and K. Wang, RSC Adv., 2019, 9, 34529 DOI: 10.1039/C9RA07201B

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