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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...

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Detalles Bibliográficos
Autores principales: Liu, Yufang, Liu, Bo, Guo, Ailing, Dong, Zhenming, Jin, Shuo, Lu, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
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.
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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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