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

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 w...

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Detalles Bibliográficos
Autores principales: Yang, Xiufang, Jiang, Xulu, Wang, Weitao, Yang, Qi, Ma, Yangmin, Wang, Kuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074145/
https://www.ncbi.nlm.nih.gov/pubmed/35529971
http://dx.doi.org/10.1039/c9ra07201b
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author Yang, Xiufang
Jiang, Xulu
Wang, Weitao
Yang, Qi
Ma, Yangmin
Wang, Kuan
author_facet Yang, Xiufang
Jiang, Xulu
Wang, Weitao
Yang, Qi
Ma, Yangmin
Wang, Kuan
author_sort Yang, Xiufang
collection PubMed
description 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.
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spelling pubmed-90741452022-05-06 Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols Yang, Xiufang Jiang, Xulu Wang, Weitao Yang, Qi Ma, Yangmin Wang, Kuan RSC Adv Chemistry 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. The Royal Society of Chemistry 2019-10-25 /pmc/articles/PMC9074145/ /pubmed/35529971 http://dx.doi.org/10.1039/c9ra07201b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yang, Xiufang
Jiang, Xulu
Wang, Weitao
Yang, Qi
Ma, Yangmin
Wang, Kuan
Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title_full Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title_fullStr Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title_full_unstemmed Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title_short Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
title_sort catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9074145/
https://www.ncbi.nlm.nih.gov/pubmed/35529971
http://dx.doi.org/10.1039/c9ra07201b
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