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Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst
The development of facile protocols for the selective synthesis of biomass-derived diamine is a highly desirable pursuit in the field of heterogeneous catalysis. Herein, a simple and highly efficient bi-functional CuNiAlO(x) catalyst was developed for the one pot transformation of 5-(hydroxymethyl)f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076022/ https://www.ncbi.nlm.nih.gov/pubmed/35540204 http://dx.doi.org/10.1039/c9ra08560b |
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author | Yuan, Hangkong Kusema, Bright T. Yan, Zhen Streiff, Stéphane Shi, Feng |
author_facet | Yuan, Hangkong Kusema, Bright T. Yan, Zhen Streiff, Stéphane Shi, Feng |
author_sort | Yuan, Hangkong |
collection | PubMed |
description | The development of facile protocols for the selective synthesis of biomass-derived diamine is a highly desirable pursuit in the field of heterogeneous catalysis. Herein, a simple and highly efficient bi-functional CuNiAlO(x) catalyst was developed for the one pot transformation of 5-(hydroxymethyl)furfural (5-HMF) into 2,5-bis(aminomethyl)furan (BAF) using a two-stage reaction process. Cu(4)Ni(1)Al(4)O(x) was found to be the most effective catalyst for this reaction, affording BAF in 85.9% yield. Our results could promote controllable conversion and utilization of biomass resource. |
format | Online Article Text |
id | pubmed-9076022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90760222022-05-09 Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst Yuan, Hangkong Kusema, Bright T. Yan, Zhen Streiff, Stéphane Shi, Feng RSC Adv Chemistry The development of facile protocols for the selective synthesis of biomass-derived diamine is a highly desirable pursuit in the field of heterogeneous catalysis. Herein, a simple and highly efficient bi-functional CuNiAlO(x) catalyst was developed for the one pot transformation of 5-(hydroxymethyl)furfural (5-HMF) into 2,5-bis(aminomethyl)furan (BAF) using a two-stage reaction process. Cu(4)Ni(1)Al(4)O(x) was found to be the most effective catalyst for this reaction, affording BAF in 85.9% yield. Our results could promote controllable conversion and utilization of biomass resource. The Royal Society of Chemistry 2019-11-27 /pmc/articles/PMC9076022/ /pubmed/35540204 http://dx.doi.org/10.1039/c9ra08560b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yuan, Hangkong Kusema, Bright T. Yan, Zhen Streiff, Stéphane Shi, Feng Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title | Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title_full | Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title_fullStr | Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title_full_unstemmed | Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title_short | Highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with NH(3) over a bifunctional catalyst |
title_sort | highly selective synthesis of 2,5-bis(aminomethyl)furan via catalytic amination of 5-(hydroxymethyl)furfural with nh(3) over a bifunctional catalyst |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076022/ https://www.ncbi.nlm.nih.gov/pubmed/35540204 http://dx.doi.org/10.1039/c9ra08560b |
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