One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment

In this study, we found a green method to obtain aryl nitriles from aromatic aldehyde in water. This simple process was modified from a conventional method. Compared with those approaches, we used water as the solvent instead of harmful chemical reagents. In this one-pot conversion, we got twenty-fi...

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Detalles Bibliográficos
Autores principales: Lin, Hongyan, Zhou, Ziling, Ma, Xiaopeng, Chen, Qingqing, Han, Hongwei, Wang, Xiaoming, Qi, Jinliang, Yang, Yonghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036638/
https://www.ncbi.nlm.nih.gov/pubmed/35479036
http://dx.doi.org/10.1039/d1ra03559b
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author Lin, Hongyan
Zhou, Ziling
Ma, Xiaopeng
Chen, Qingqing
Han, Hongwei
Wang, Xiaoming
Qi, Jinliang
Yang, Yonghua
author_facet Lin, Hongyan
Zhou, Ziling
Ma, Xiaopeng
Chen, Qingqing
Han, Hongwei
Wang, Xiaoming
Qi, Jinliang
Yang, Yonghua
author_sort Lin, Hongyan
collection PubMed
description In this study, we found a green method to obtain aryl nitriles from aromatic aldehyde in water. This simple process was modified from a conventional method. Compared with those approaches, we used water as the solvent instead of harmful chemical reagents. In this one-pot conversion, we got twenty-five aryl nitriles conveniently with pollution to the environment being minimized. Furthermore, we confirmed the reaction mechanism by capturing the intermediates, aldoximes.
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spelling pubmed-90366382022-04-26 One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment Lin, Hongyan Zhou, Ziling Ma, Xiaopeng Chen, Qingqing Han, Hongwei Wang, Xiaoming Qi, Jinliang Yang, Yonghua RSC Adv Chemistry In this study, we found a green method to obtain aryl nitriles from aromatic aldehyde in water. This simple process was modified from a conventional method. Compared with those approaches, we used water as the solvent instead of harmful chemical reagents. In this one-pot conversion, we got twenty-five aryl nitriles conveniently with pollution to the environment being minimized. Furthermore, we confirmed the reaction mechanism by capturing the intermediates, aldoximes. The Royal Society of Chemistry 2021-07-09 /pmc/articles/PMC9036638/ /pubmed/35479036 http://dx.doi.org/10.1039/d1ra03559b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Lin, Hongyan
Zhou, Ziling
Ma, Xiaopeng
Chen, Qingqing
Han, Hongwei
Wang, Xiaoming
Qi, Jinliang
Yang, Yonghua
One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title_full One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title_fullStr One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title_full_unstemmed One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title_short One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
title_sort one pot synthesis of aryl nitriles from aromatic aldehydes in a water environment
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036638/
https://www.ncbi.nlm.nih.gov/pubmed/35479036
http://dx.doi.org/10.1039/d1ra03559b
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