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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...

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Detalles Bibliográficos
Autores principales: Streng, Emilia S, Lee, Darren S, George, Michael W, Poliakoff, Martyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
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.
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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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