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Protocol for microwave-assisted synthesis of unsymmetrical azo dyes

Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW...

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Detalles Bibliográficos
Autores principales: Thakuri, Ankit, Banerjee, Mainak, Chatterjee, Amrita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678771/
https://www.ncbi.nlm.nih.gov/pubmed/36595940
http://dx.doi.org/10.1016/j.xpro.2022.101864
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author Thakuri, Ankit
Banerjee, Mainak
Chatterjee, Amrita
author_facet Thakuri, Ankit
Banerjee, Mainak
Chatterjee, Amrita
author_sort Thakuri, Ankit
collection PubMed
description Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW)-assisted protocol for rapid access to a large variety of unsymmetrical azo dyes by coupling nitroarenes and aromatic amines. After MW-assisted coupling, the azo dyes are then isolated by precipitation followed by recrystallization to obtain pure azo dyes. For complete details on the use and execution of this protocol, please refer to Thakuri et al. (2022).(1)
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spelling pubmed-96787712022-11-23 Protocol for microwave-assisted synthesis of unsymmetrical azo dyes Thakuri, Ankit Banerjee, Mainak Chatterjee, Amrita STAR Protoc Protocol Aromatic azo dyes bear immense commercial significance because of their extensive usage in the textile, paint, and food industries. With growing environmental concerns, developing alternative greener approaches for the synthesis of azo dyes is crucial. Herein, we describe a metal-free, microwave (MW)-assisted protocol for rapid access to a large variety of unsymmetrical azo dyes by coupling nitroarenes and aromatic amines. After MW-assisted coupling, the azo dyes are then isolated by precipitation followed by recrystallization to obtain pure azo dyes. For complete details on the use and execution of this protocol, please refer to Thakuri et al. (2022).(1) Elsevier 2022-11-17 /pmc/articles/PMC9678771/ /pubmed/36595940 http://dx.doi.org/10.1016/j.xpro.2022.101864 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Thakuri, Ankit
Banerjee, Mainak
Chatterjee, Amrita
Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title_full Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title_fullStr Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title_full_unstemmed Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title_short Protocol for microwave-assisted synthesis of unsymmetrical azo dyes
title_sort protocol for microwave-assisted synthesis of unsymmetrical azo dyes
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9678771/
https://www.ncbi.nlm.nih.gov/pubmed/36595940
http://dx.doi.org/10.1016/j.xpro.2022.101864
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