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Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts

A new method for the direct synthesis of primary and secondary amides from carboxylic acids is described using Mg(NO(3))(2)·6H(2)O or imidazole as a low-cost and readily available catalyst, and urea as a stable, and easy to manipulate nitrogen source. This methodology is particularly useful for the...

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Autores principales: Chhatwal, A. Rosie, Lomax, Helen V., Blacker, A. John, Williams, Jonathan M. J., Marcé, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416778/
https://www.ncbi.nlm.nih.gov/pubmed/32832055
http://dx.doi.org/10.1039/d0sc01317j
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author Chhatwal, A. Rosie
Lomax, Helen V.
Blacker, A. John
Williams, Jonathan M. J.
Marcé, Patricia
author_facet Chhatwal, A. Rosie
Lomax, Helen V.
Blacker, A. John
Williams, Jonathan M. J.
Marcé, Patricia
author_sort Chhatwal, A. Rosie
collection PubMed
description A new method for the direct synthesis of primary and secondary amides from carboxylic acids is described using Mg(NO(3))(2)·6H(2)O or imidazole as a low-cost and readily available catalyst, and urea as a stable, and easy to manipulate nitrogen source. This methodology is particularly useful for the direct synthesis of primary and methyl amides avoiding the use of ammonia and methylamine gas which can be tedious to manipulate. Furthermore, the transformation does not require the employment of coupling or activating agents which are commonly required.
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spelling pubmed-74167782020-08-20 Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts Chhatwal, A. Rosie Lomax, Helen V. Blacker, A. John Williams, Jonathan M. J. Marcé, Patricia Chem Sci Chemistry A new method for the direct synthesis of primary and secondary amides from carboxylic acids is described using Mg(NO(3))(2)·6H(2)O or imidazole as a low-cost and readily available catalyst, and urea as a stable, and easy to manipulate nitrogen source. This methodology is particularly useful for the direct synthesis of primary and methyl amides avoiding the use of ammonia and methylamine gas which can be tedious to manipulate. Furthermore, the transformation does not require the employment of coupling or activating agents which are commonly required. Royal Society of Chemistry 2020-05-19 /pmc/articles/PMC7416778/ /pubmed/32832055 http://dx.doi.org/10.1039/d0sc01317j Text en This journal is © The Royal Society of Chemistry 2020 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Chhatwal, A. Rosie
Lomax, Helen V.
Blacker, A. John
Williams, Jonathan M. J.
Marcé, Patricia
Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title_full Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title_fullStr Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title_full_unstemmed Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title_short Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO(3))(2) or imidazole as catalysts
title_sort direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and mg(no(3))(2) or imidazole as catalysts
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7416778/
https://www.ncbi.nlm.nih.gov/pubmed/32832055
http://dx.doi.org/10.1039/d0sc01317j
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