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A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst
A heterogeneous copper-catalyzed A(3) coupling reaction of aldehydes, amines, and alkynes for the synthesis of propargylamines and benzofurans has been developed. Here, the modified metal–organic framework MIL-101(Cr)-SB-Cu complex was chosen as the heterogeneous copper catalyst and prepared via pos...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412598/ https://www.ncbi.nlm.nih.gov/pubmed/37558730 http://dx.doi.org/10.1038/s41598-023-40154-0 |
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author | Sarkar, Fillip Kumar Kyndiah, Lenida Gajurel, Sushmita Sarkar, Rajib Jana, Samaresh Pal, Amarta Kumar |
author_facet | Sarkar, Fillip Kumar Kyndiah, Lenida Gajurel, Sushmita Sarkar, Rajib Jana, Samaresh Pal, Amarta Kumar |
author_sort | Sarkar, Fillip Kumar |
collection | PubMed |
description | A heterogeneous copper-catalyzed A(3) coupling reaction of aldehydes, amines, and alkynes for the synthesis of propargylamines and benzofurans has been developed. Here, the modified metal–organic framework MIL-101(Cr)-SB-Cu complex was chosen as the heterogeneous copper catalyst and prepared via post-synthetic modification of amino-functionalized MIL-101(Cr). The structure, morphology, thermal stability, and copper content of the catalyst were determined by FT-IR, PXRD, SEM, TEM, EDX, TGA, XPS, and ICP-OES. The catalyst shows high catalytic activity for the aforementioned reactions under solvent-free reaction conditions. High yields, low catalyst loading, easy catalyst recovery and reusability with not much shrink in catalytic activity, and a good yield of 82% in gram-scale synthesis are some of the benefits of this protocol that drove it towards sustainability. |
format | Online Article Text |
id | pubmed-10412598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104125982023-08-11 A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst Sarkar, Fillip Kumar Kyndiah, Lenida Gajurel, Sushmita Sarkar, Rajib Jana, Samaresh Pal, Amarta Kumar Sci Rep Article A heterogeneous copper-catalyzed A(3) coupling reaction of aldehydes, amines, and alkynes for the synthesis of propargylamines and benzofurans has been developed. Here, the modified metal–organic framework MIL-101(Cr)-SB-Cu complex was chosen as the heterogeneous copper catalyst and prepared via post-synthetic modification of amino-functionalized MIL-101(Cr). The structure, morphology, thermal stability, and copper content of the catalyst were determined by FT-IR, PXRD, SEM, TEM, EDX, TGA, XPS, and ICP-OES. The catalyst shows high catalytic activity for the aforementioned reactions under solvent-free reaction conditions. High yields, low catalyst loading, easy catalyst recovery and reusability with not much shrink in catalytic activity, and a good yield of 82% in gram-scale synthesis are some of the benefits of this protocol that drove it towards sustainability. Nature Publishing Group UK 2023-08-09 /pmc/articles/PMC10412598/ /pubmed/37558730 http://dx.doi.org/10.1038/s41598-023-40154-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sarkar, Fillip Kumar Kyndiah, Lenida Gajurel, Sushmita Sarkar, Rajib Jana, Samaresh Pal, Amarta Kumar A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title | A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title_full | A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title_fullStr | A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title_full_unstemmed | A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title_short | A sustainable avenue for the synthesis of propargylamines and benzofurans using a Cu-functionalized MIL-101(Cr) as a reusable heterogeneous catalyst |
title_sort | sustainable avenue for the synthesis of propargylamines and benzofurans using a cu-functionalized mil-101(cr) as a reusable heterogeneous catalyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412598/ https://www.ncbi.nlm.nih.gov/pubmed/37558730 http://dx.doi.org/10.1038/s41598-023-40154-0 |
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