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Generation and Trapping of Ketenes in Flow
Ketenes were generated by the thermolysis of alkoxyalkynes under flow conditions, and then trapped with amines and alcohols to cleanly give amides and esters. For a 10 min reaction time, temperatures of 180, 160, and 140 °C were required for >95 % conversion of EtO, iPrO, and tBuO alkoxyalkynes,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464552/ https://www.ncbi.nlm.nih.gov/pubmed/26097406 http://dx.doi.org/10.1002/ejoc.201403603 |
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author | Henry, Cyril Bolien, David Ibanescu, Bogdan Bloodworth, Sally Harrowven, David C Zhang, Xunli Craven, Andy Sneddon, Helen F Whitby, Richard J |
author_facet | Henry, Cyril Bolien, David Ibanescu, Bogdan Bloodworth, Sally Harrowven, David C Zhang, Xunli Craven, Andy Sneddon, Helen F Whitby, Richard J |
author_sort | Henry, Cyril |
collection | PubMed |
description | Ketenes were generated by the thermolysis of alkoxyalkynes under flow conditions, and then trapped with amines and alcohols to cleanly give amides and esters. For a 10 min reaction time, temperatures of 180, 160, and 140 °C were required for >95 % conversion of EtO, iPrO, and tBuO alkoxyalkynes, respectively. Variation of the temperature and flow rate with inline monitoring of the output by IR spectroscopy allowed the kinetic parameters for the conversion of 1-ethoxy-1-octyne to be easily estimated (E(a) = 105.4 kJ/mol). Trapping of the in-situ-generated ketenes by alcohols to give esters required the addition of a tertiary amine catalyst to prevent competitive [2+2] addition of the ketene to the alkoxyalkyne precursor. |
format | Online Article Text |
id | pubmed-4464552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-44645522015-06-17 Generation and Trapping of Ketenes in Flow Henry, Cyril Bolien, David Ibanescu, Bogdan Bloodworth, Sally Harrowven, David C Zhang, Xunli Craven, Andy Sneddon, Helen F Whitby, Richard J European J Org Chem Full Papers Ketenes were generated by the thermolysis of alkoxyalkynes under flow conditions, and then trapped with amines and alcohols to cleanly give amides and esters. For a 10 min reaction time, temperatures of 180, 160, and 140 °C were required for >95 % conversion of EtO, iPrO, and tBuO alkoxyalkynes, respectively. Variation of the temperature and flow rate with inline monitoring of the output by IR spectroscopy allowed the kinetic parameters for the conversion of 1-ethoxy-1-octyne to be easily estimated (E(a) = 105.4 kJ/mol). Trapping of the in-situ-generated ketenes by alcohols to give esters required the addition of a tertiary amine catalyst to prevent competitive [2+2] addition of the ketene to the alkoxyalkyne precursor. WILEY-VCH Verlag 2015-03 2015-01-20 /pmc/articles/PMC4464552/ /pubmed/26097406 http://dx.doi.org/10.1002/ejoc.201403603 Text en © 2015 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Henry, Cyril Bolien, David Ibanescu, Bogdan Bloodworth, Sally Harrowven, David C Zhang, Xunli Craven, Andy Sneddon, Helen F Whitby, Richard J Generation and Trapping of Ketenes in Flow |
title | Generation and Trapping of Ketenes in Flow |
title_full | Generation and Trapping of Ketenes in Flow |
title_fullStr | Generation and Trapping of Ketenes in Flow |
title_full_unstemmed | Generation and Trapping of Ketenes in Flow |
title_short | Generation and Trapping of Ketenes in Flow |
title_sort | generation and trapping of ketenes in flow |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464552/ https://www.ncbi.nlm.nih.gov/pubmed/26097406 http://dx.doi.org/10.1002/ejoc.201403603 |
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