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Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water
The synthesis of the azoxybenzenes by the reduction of nitroarenes with reducing agent potassium borohydride in water was reported for the first time. PEG-400 was used as a phase transfer catalyst and could effectively catalyze the reduction. The electronic effects of substituent groups play an impo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263276/ https://www.ncbi.nlm.nih.gov/pubmed/21527883 http://dx.doi.org/10.3390/molecules16053563 |
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author | Liu, Yufang Liu, Bo Guo, Ailing Dong, Zhenming Jin, Shuo Lu, Yun |
author_facet | Liu, Yufang Liu, Bo Guo, Ailing Dong, Zhenming Jin, Shuo Lu, Yun |
author_sort | Liu, Yufang |
collection | PubMed |
description | The synthesis of the azoxybenzenes by the reduction of nitroarenes with reducing agent potassium borohydride in water was reported for the first time. PEG-400 was used as a phase transfer catalyst and could effectively catalyze the reduction. The electronic effects of substituent groups play an important role in determining the reduction efficiencies. Electron-withdrawing substituents promote the formation of the azoxybenzene products, while electron-releasing groups retard the reductions to various degrees depending on the extent of their electron-donating ability. |
format | Online Article Text |
id | pubmed-6263276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62632762018-12-10 Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water Liu, Yufang Liu, Bo Guo, Ailing Dong, Zhenming Jin, Shuo Lu, Yun Molecules Communication The synthesis of the azoxybenzenes by the reduction of nitroarenes with reducing agent potassium borohydride in water was reported for the first time. PEG-400 was used as a phase transfer catalyst and could effectively catalyze the reduction. The electronic effects of substituent groups play an important role in determining the reduction efficiencies. Electron-withdrawing substituents promote the formation of the azoxybenzene products, while electron-releasing groups retard the reductions to various degrees depending on the extent of their electron-donating ability. MDPI 2011-04-28 /pmc/articles/PMC6263276/ /pubmed/21527883 http://dx.doi.org/10.3390/molecules16053563 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Communication Liu, Yufang Liu, Bo Guo, Ailing Dong, Zhenming Jin, Shuo Lu, Yun Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title | Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title_full | Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title_fullStr | Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title_full_unstemmed | Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title_short | Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water |
title_sort | reduction of nitroarenes to azoxybenzenes by potassium borohydride in water |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263276/ https://www.ncbi.nlm.nih.gov/pubmed/21527883 http://dx.doi.org/10.3390/molecules16053563 |
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