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Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2)
The use of γ-Al(2)O(3) as a heterogeneous catalyst in scCO(2) has been successfully applied to the amination of alcohols for the synthesis of N-alkylated heterocycles. The optimal reaction conditions (temperature and substrate flow rate) were determined using an automated self-optimising reactor, re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331277/ https://www.ncbi.nlm.nih.gov/pubmed/28326142 http://dx.doi.org/10.3762/bjoc.13.36 |
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author | Streng, Emilia S Lee, Darren S George, Michael W Poliakoff, Martyn |
author_facet | Streng, Emilia S Lee, Darren S George, Michael W Poliakoff, Martyn |
author_sort | Streng, Emilia S |
collection | PubMed |
description | The use of γ-Al(2)O(3) as a heterogeneous catalyst in scCO(2) has been successfully applied to the amination of alcohols for the synthesis of N-alkylated heterocycles. The optimal reaction conditions (temperature and substrate flow rate) were determined using an automated self-optimising reactor, resulting in moderate to high yields of the target products. Carrying out the reaction in scCO(2) was shown to be beneficial, as higher yields were obtained in the presence of CO(2) than in its absence. A surprising discovery is that, in addition to cyclic amines, cyclic ureas and urethanes could be synthesised by incorporation of CO(2) from the supercritical solvent into the product. |
format | Online Article Text |
id | pubmed-5331277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-53312772017-03-21 Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) Streng, Emilia S Lee, Darren S George, Michael W Poliakoff, Martyn Beilstein J Org Chem Full Research Paper The use of γ-Al(2)O(3) as a heterogeneous catalyst in scCO(2) has been successfully applied to the amination of alcohols for the synthesis of N-alkylated heterocycles. The optimal reaction conditions (temperature and substrate flow rate) were determined using an automated self-optimising reactor, resulting in moderate to high yields of the target products. Carrying out the reaction in scCO(2) was shown to be beneficial, as higher yields were obtained in the presence of CO(2) than in its absence. A surprising discovery is that, in addition to cyclic amines, cyclic ureas and urethanes could be synthesised by incorporation of CO(2) from the supercritical solvent into the product. Beilstein-Institut 2017-02-21 /pmc/articles/PMC5331277/ /pubmed/28326142 http://dx.doi.org/10.3762/bjoc.13.36 Text en Copyright © 2017, Streng et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Streng, Emilia S Lee, Darren S George, Michael W Poliakoff, Martyn Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title | Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title_full | Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title_fullStr | Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title_full_unstemmed | Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title_short | Continuous N-alkylation reactions of amino alcohols using γ-Al(2)O(3) and supercritical CO(2): unexpected formation of cyclic ureas and urethanes by reaction with CO(2) |
title_sort | continuous n-alkylation reactions of amino alcohols using γ-al(2)o(3) and supercritical co(2): unexpected formation of cyclic ureas and urethanes by reaction with co(2) |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5331277/ https://www.ncbi.nlm.nih.gov/pubmed/28326142 http://dx.doi.org/10.3762/bjoc.13.36 |
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