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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
Descripción
Sumario: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.