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Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols
An efficient and direct protocol for the preparation of amidoalkylnaphthols employing a multi-component, one-pot condensation reaction of 2-naphthol, aromatic aldehydes and acetamide or benzamide in the presence of graphite supported perchloric acid under solvent-free conditions is described. The th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270571/ https://www.ncbi.nlm.nih.gov/pubmed/23358323 http://dx.doi.org/10.3390/molecules18021653 |
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author | Lei, Zhen-Kai Xiao, Li Lu, Xiao-Quan Huang, He Liu, Chen-Jiang |
author_facet | Lei, Zhen-Kai Xiao, Li Lu, Xiao-Quan Huang, He Liu, Chen-Jiang |
author_sort | Lei, Zhen-Kai |
collection | PubMed |
description | An efficient and direct protocol for the preparation of amidoalkylnaphthols employing a multi-component, one-pot condensation reaction of 2-naphthol, aromatic aldehydes and acetamide or benzamide in the presence of graphite supported perchloric acid under solvent-free conditions is described. The thermal solvent-free procedure offers advantages such as simple work-up, shorter reaction times and higher product yields, and the catalyst exhibited remarkable reactivity and can be recycled. |
format | Online Article Text |
id | pubmed-6270571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62705712018-12-14 Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols Lei, Zhen-Kai Xiao, Li Lu, Xiao-Quan Huang, He Liu, Chen-Jiang Molecules Article An efficient and direct protocol for the preparation of amidoalkylnaphthols employing a multi-component, one-pot condensation reaction of 2-naphthol, aromatic aldehydes and acetamide or benzamide in the presence of graphite supported perchloric acid under solvent-free conditions is described. The thermal solvent-free procedure offers advantages such as simple work-up, shorter reaction times and higher product yields, and the catalyst exhibited remarkable reactivity and can be recycled. MDPI 2013-01-28 /pmc/articles/PMC6270571/ /pubmed/23358323 http://dx.doi.org/10.3390/molecules18021653 Text en © 2013 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 Lei, Zhen-Kai Xiao, Li Lu, Xiao-Quan Huang, He Liu, Chen-Jiang Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title | Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title_full | Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title_fullStr | Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title_full_unstemmed | Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title_short | Graphite-Supported Perchloric Acid (HClO(4)-C): An Efficient and Recyclable Heterogeneous Catalyst for the One-Pot Synthesis of Amidoalkyl Naphthols |
title_sort | graphite-supported perchloric acid (hclo(4)-c): an efficient and recyclable heterogeneous catalyst for the one-pot synthesis of amidoalkyl naphthols |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270571/ https://www.ncbi.nlm.nih.gov/pubmed/23358323 http://dx.doi.org/10.3390/molecules18021653 |
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