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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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. |
format | Online Article Text |
id | pubmed-9074145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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