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Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction

A simple deep eutectic solvent based on tin (II) chloride was used as a dual catalyst and environmentally benign reaction medium for an efficient synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives, from aromatic and aliphatic aldehydes, 1,3-dicarbonyl compounds, and urea in good-to-excellent yi...

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Autores principales: Azizi, Najmadin, Dezfuli, Sahar, Hahsemi, Mohmmad Mahmoodi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific World Journal 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350898/
https://www.ncbi.nlm.nih.gov/pubmed/22649326
http://dx.doi.org/10.1100/2012/908702
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author Azizi, Najmadin
Dezfuli, Sahar
Hahsemi, Mohmmad Mahmoodi
author_facet Azizi, Najmadin
Dezfuli, Sahar
Hahsemi, Mohmmad Mahmoodi
author_sort Azizi, Najmadin
collection PubMed
description A simple deep eutectic solvent based on tin (II) chloride was used as a dual catalyst and environmentally benign reaction medium for an efficient synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives, from aromatic and aliphatic aldehydes, 1,3-dicarbonyl compounds, and urea in good-to-excellent yields and short reaction time. This simple ammonium deep eutectic solvent, easily synthesized from choline chloride and tin chloride, is relatively inexpensive and recyclable, making it applicable for industrial applications.
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spelling pubmed-33508982012-05-30 Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction Azizi, Najmadin Dezfuli, Sahar Hahsemi, Mohmmad Mahmoodi ScientificWorldJournal Research Article A simple deep eutectic solvent based on tin (II) chloride was used as a dual catalyst and environmentally benign reaction medium for an efficient synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives, from aromatic and aliphatic aldehydes, 1,3-dicarbonyl compounds, and urea in good-to-excellent yields and short reaction time. This simple ammonium deep eutectic solvent, easily synthesized from choline chloride and tin chloride, is relatively inexpensive and recyclable, making it applicable for industrial applications. The Scientific World Journal 2012-04-29 /pmc/articles/PMC3350898/ /pubmed/22649326 http://dx.doi.org/10.1100/2012/908702 Text en Copyright © 2012 Najmadin Azizi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Azizi, Najmadin
Dezfuli, Sahar
Hahsemi, Mohmmad Mahmoodi
Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title_full Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title_fullStr Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title_full_unstemmed Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title_short Eutectic Salt Catalyzed Environmentally Benign and Highly Efficient Biginelli Reaction
title_sort eutectic salt catalyzed environmentally benign and highly efficient biginelli reaction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350898/
https://www.ncbi.nlm.nih.gov/pubmed/22649326
http://dx.doi.org/10.1100/2012/908702
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