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Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water

Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs) based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18) and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liqu...

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Detalles Bibliográficos
Autores principales: He, Leqin, Qin, Shenjun, Chang, Tao, Sun, Yuzhuang, Zhao, Jiquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057752/
https://www.ncbi.nlm.nih.gov/pubmed/24837832
http://dx.doi.org/10.3390/ijms15058656
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author He, Leqin
Qin, Shenjun
Chang, Tao
Sun, Yuzhuang
Zhao, Jiquan
author_facet He, Leqin
Qin, Shenjun
Chang, Tao
Sun, Yuzhuang
Zhao, Jiquan
author_sort He, Leqin
collection PubMed
description Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs) based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18) and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liquids were applied in three-component Mannich reactions with an aldehyde, ketone, and amine at 25 °C in water. The effects of the type and amount of catalyst and reaction time as well as the scope of the reaction were investigated. Results showed that GBAIL-C(14) has excellent catalytic activity and fair reusability. The catalytic procedure was simple, and the catalyst could be recycled seven times via a simple separation process without noticeable decreases in catalytic activity.
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spelling pubmed-40577522014-06-16 Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water He, Leqin Qin, Shenjun Chang, Tao Sun, Yuzhuang Zhao, Jiquan Int J Mol Sci Article Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs) based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18) and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liquids were applied in three-component Mannich reactions with an aldehyde, ketone, and amine at 25 °C in water. The effects of the type and amount of catalyst and reaction time as well as the scope of the reaction were investigated. Results showed that GBAIL-C(14) has excellent catalytic activity and fair reusability. The catalytic procedure was simple, and the catalyst could be recycled seven times via a simple separation process without noticeable decreases in catalytic activity. Molecular Diversity Preservation International (MDPI) 2014-05-15 /pmc/articles/PMC4057752/ /pubmed/24837832 http://dx.doi.org/10.3390/ijms15058656 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
He, Leqin
Qin, Shenjun
Chang, Tao
Sun, Yuzhuang
Zhao, Jiquan
Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title_full Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title_fullStr Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title_full_unstemmed Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title_short Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
title_sort geminal brønsted acid ionic liquids as catalysts for the mannich reaction in water
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057752/
https://www.ncbi.nlm.nih.gov/pubmed/24837832
http://dx.doi.org/10.3390/ijms15058656
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