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Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry
Anilines are important feedstocks for pharmaceuticals, dyes, and other materials, but traditional approaches to their syntheses usually lack selectivity and environmental sustainability. Here, we describe the selective reduction of nitrobenzene to aniline under mild conditions, using water as the ul...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641269/ https://www.ncbi.nlm.nih.gov/pubmed/36386882 http://dx.doi.org/10.1016/j.xpro.2022.101817 |
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author | Stergiou, Athanasios D. Broadhurst, Daniel H. Symes, Mark D. |
author_facet | Stergiou, Athanasios D. Broadhurst, Daniel H. Symes, Mark D. |
author_sort | Stergiou, Athanasios D. |
collection | PubMed |
description | Anilines are important feedstocks for pharmaceuticals, dyes, and other materials, but traditional approaches to their syntheses usually lack selectivity and environmental sustainability. Here, we describe the selective reduction of nitrobenzene to aniline under mild conditions, using water as the ultimate source of the required protons and electrons. We describe the electrochemical cell assembly, and detail steps for electrochemical reduction followed by organic extraction and analysis of the extracts using NMR. For complete details on the use and execution of this protocol, please refer to Stergiou and Symes (2022a). |
format | Online Article Text |
id | pubmed-9641269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96412692022-11-15 Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry Stergiou, Athanasios D. Broadhurst, Daniel H. Symes, Mark D. STAR Protoc Protocol Anilines are important feedstocks for pharmaceuticals, dyes, and other materials, but traditional approaches to their syntheses usually lack selectivity and environmental sustainability. Here, we describe the selective reduction of nitrobenzene to aniline under mild conditions, using water as the ultimate source of the required protons and electrons. We describe the electrochemical cell assembly, and detail steps for electrochemical reduction followed by organic extraction and analysis of the extracts using NMR. For complete details on the use and execution of this protocol, please refer to Stergiou and Symes (2022a). Elsevier 2022-11-04 /pmc/articles/PMC9641269/ /pubmed/36386882 http://dx.doi.org/10.1016/j.xpro.2022.101817 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Stergiou, Athanasios D. Broadhurst, Daniel H. Symes, Mark D. Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title | Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title_full | Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title_fullStr | Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title_full_unstemmed | Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title_short | Electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
title_sort | electrochemical reduction of nitrobenzene via redox-mediated chronoamperometry |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641269/ https://www.ncbi.nlm.nih.gov/pubmed/36386882 http://dx.doi.org/10.1016/j.xpro.2022.101817 |
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