Cargando…
N-Dimethylation and N-Functionalization of Amines Using Ru Nanoparticle Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source
[Image: see text] N-methylated amines are essential bioactive compounds and have been widely used in the fine and bulk chemical industries, as well as in pharmaceuticals, agrochemicals, and dyes. Developing green, efficient, and low-cost catalysts for methylation of amines by using efficient and eas...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427653/ https://www.ncbi.nlm.nih.gov/pubmed/34514223 http://dx.doi.org/10.1021/acsomega.1c01961 |
_version_ | 1783750220573573120 |
---|---|
author | Liu, Jianguo Song, Yanpei Wu, Xiang Ma, Longlong |
author_facet | Liu, Jianguo Song, Yanpei Wu, Xiang Ma, Longlong |
author_sort | Liu, Jianguo |
collection | PubMed |
description | [Image: see text] N-methylated amines are essential bioactive compounds and have been widely used in the fine and bulk chemical industries, as well as in pharmaceuticals, agrochemicals, and dyes. Developing green, efficient, and low-cost catalysts for methylation of amines by using efficient and easily accessible methylating reagents is highly desired yet remains a significant challenge. Herein, we report the selective N-dimethylation of different functional amines with different functional aldehydes under easy-to-handle and industrially applicable conditions using carbon-supported Ru nanoparticles (Ru/C) as a heterogeneous catalyst. A broad spectrum of amines could be efficiently converted to their corresponding N,N-dimethyl amines with good compatibility of various functional groups. This method is widely applicable to N-dimethylation of primary amines including aromatic, aliphatic amines with formaldehyde, and synthesis of tertiary amines from primary, secondary amines with different functional aldehydes. The advantage of this newly described method includes operational simplicity, high turnover number, the ready availability of the catalyst, and good functional group compatibility. This Ru/C catalyzed N-dimethylation reaction possibly proceeds through a two-step N-methylation reaction process. |
format | Online Article Text |
id | pubmed-8427653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84276532021-09-10 N-Dimethylation and N-Functionalization of Amines Using Ru Nanoparticle Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source Liu, Jianguo Song, Yanpei Wu, Xiang Ma, Longlong ACS Omega [Image: see text] N-methylated amines are essential bioactive compounds and have been widely used in the fine and bulk chemical industries, as well as in pharmaceuticals, agrochemicals, and dyes. Developing green, efficient, and low-cost catalysts for methylation of amines by using efficient and easily accessible methylating reagents is highly desired yet remains a significant challenge. Herein, we report the selective N-dimethylation of different functional amines with different functional aldehydes under easy-to-handle and industrially applicable conditions using carbon-supported Ru nanoparticles (Ru/C) as a heterogeneous catalyst. A broad spectrum of amines could be efficiently converted to their corresponding N,N-dimethyl amines with good compatibility of various functional groups. This method is widely applicable to N-dimethylation of primary amines including aromatic, aliphatic amines with formaldehyde, and synthesis of tertiary amines from primary, secondary amines with different functional aldehydes. The advantage of this newly described method includes operational simplicity, high turnover number, the ready availability of the catalyst, and good functional group compatibility. This Ru/C catalyzed N-dimethylation reaction possibly proceeds through a two-step N-methylation reaction process. American Chemical Society 2021-08-26 /pmc/articles/PMC8427653/ /pubmed/34514223 http://dx.doi.org/10.1021/acsomega.1c01961 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Liu, Jianguo Song, Yanpei Wu, Xiang Ma, Longlong N-Dimethylation and N-Functionalization of Amines Using Ru Nanoparticle Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title | N-Dimethylation and N-Functionalization
of Amines Using Ru Nanoparticle
Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title_full | N-Dimethylation and N-Functionalization
of Amines Using Ru Nanoparticle
Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title_fullStr | N-Dimethylation and N-Functionalization
of Amines Using Ru Nanoparticle
Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title_full_unstemmed | N-Dimethylation and N-Functionalization
of Amines Using Ru Nanoparticle
Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title_short | N-Dimethylation and N-Functionalization
of Amines Using Ru Nanoparticle
Catalysts and Formaldehyde or Functional Aldehydes as the Carbon Source |
title_sort | n-dimethylation and n-functionalization
of amines using ru nanoparticle
catalysts and formaldehyde or functional aldehydes as the carbon source |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8427653/ https://www.ncbi.nlm.nih.gov/pubmed/34514223 http://dx.doi.org/10.1021/acsomega.1c01961 |
work_keys_str_mv | AT liujianguo ndimethylationandnfunctionalizationofaminesusingrunanoparticlecatalystsandformaldehydeorfunctionalaldehydesasthecarbonsource AT songyanpei ndimethylationandnfunctionalizationofaminesusingrunanoparticlecatalystsandformaldehydeorfunctionalaldehydesasthecarbonsource AT wuxiang ndimethylationandnfunctionalizationofaminesusingrunanoparticlecatalystsandformaldehydeorfunctionalaldehydesasthecarbonsource AT malonglong ndimethylationandnfunctionalizationofaminesusingrunanoparticlecatalystsandformaldehydeorfunctionalaldehydesasthecarbonsource |