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A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions
Our main goal in this work is to synthesize valuable sulfonamide compounds according to the principles of green chemistry and also to present a unique convergent paired mechanism for their synthesis. In this study, we introduced a new type of convergent paired electro-organic synthesis of sulfonamid...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579442/ https://www.ncbi.nlm.nih.gov/pubmed/37845371 http://dx.doi.org/10.1038/s41598-023-44912-y |
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author | Patoghi, Pouria Sadatnabi, Ali Nematollahi, Davood |
author_facet | Patoghi, Pouria Sadatnabi, Ali Nematollahi, Davood |
author_sort | Patoghi, Pouria |
collection | PubMed |
description | Our main goal in this work is to synthesize valuable sulfonamide compounds according to the principles of green chemistry and also to present a unique convergent paired mechanism for their synthesis. In this study, we introduced a new type of convergent paired electro-organic synthesis of sulfonamide derivatives via a catalyst, oxidant, halogen and amine-free method. In this research, instead of using toxic amine compounds, an innovative mechanism based on the reduction of nitro compounds and in-situ production of amine compounds was used. The mechanism of electrophile generation is the cathodic reduction of the nitro compound to the hydroxylamine compound and then the anodic oxidation of the hydroxylamine to the nitroso compound. On the other hand, the nucleophile generation mechanism involves the two-electron oxidation of sulfonyl hydrazide to related sulfinic acid at the anode surface. The reaction leading to the synthesis of sulfonamides involves a one-pot reaction of the generated nitroso compound with the produced sulfinic compound. |
format | Online Article Text |
id | pubmed-10579442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105794422023-10-18 A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions Patoghi, Pouria Sadatnabi, Ali Nematollahi, Davood Sci Rep Article Our main goal in this work is to synthesize valuable sulfonamide compounds according to the principles of green chemistry and also to present a unique convergent paired mechanism for their synthesis. In this study, we introduced a new type of convergent paired electro-organic synthesis of sulfonamide derivatives via a catalyst, oxidant, halogen and amine-free method. In this research, instead of using toxic amine compounds, an innovative mechanism based on the reduction of nitro compounds and in-situ production of amine compounds was used. The mechanism of electrophile generation is the cathodic reduction of the nitro compound to the hydroxylamine compound and then the anodic oxidation of the hydroxylamine to the nitroso compound. On the other hand, the nucleophile generation mechanism involves the two-electron oxidation of sulfonyl hydrazide to related sulfinic acid at the anode surface. The reaction leading to the synthesis of sulfonamides involves a one-pot reaction of the generated nitroso compound with the produced sulfinic compound. Nature Publishing Group UK 2023-10-16 /pmc/articles/PMC10579442/ /pubmed/37845371 http://dx.doi.org/10.1038/s41598-023-44912-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Patoghi, Pouria Sadatnabi, Ali Nematollahi, Davood A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title | A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title_full | A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title_fullStr | A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title_full_unstemmed | A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title_short | A new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
title_sort | new type of convergent paired electrochemical synthesis of sulfonamides under green and catalyst-free conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579442/ https://www.ncbi.nlm.nih.gov/pubmed/37845371 http://dx.doi.org/10.1038/s41598-023-44912-y |
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