Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers
Production of glycidyl ethers is industrially carried Out by reacting alcohols with epichlorhydrin, a potentially carcinogenic compound. This paper investigates a less hazardous alternative-that of a chemo-enzymatic process in which Candida antarctica lipase B catalysed generation of peracid from a...
Published in: | Journal of Molecular Catalysis B: Enzymatic |
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Main Authors: | , , , , |
Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Elsevier
2008
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Subjects: | |
Online Access: | https://lup.lub.lu.se/record/1254666 https://doi.org/10.1016/j.molcatb.2007.11.015 https://portal.research.lu.se/files/2825436/1268339.pdf |
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author | Tufvesson, Pär Adlercreutz, Dietlind Lundmark, Stefan Manea, Mircea Hatti-Kaul, Rajni |
author_facet | Tufvesson, Pär Adlercreutz, Dietlind Lundmark, Stefan Manea, Mircea Hatti-Kaul, Rajni |
author_sort | Tufvesson, Pär |
collection | Lund University Publications (LUP) |
container_issue | 1-2 |
container_start_page | 1 |
container_title | Journal of Molecular Catalysis B: Enzymatic |
container_volume | 54 |
description | Production of glycidyl ethers is industrially carried Out by reacting alcohols with epichlorhydrin, a potentially carcinogenic compound. This paper investigates a less hazardous alternative-that of a chemo-enzymatic process in which Candida antarctica lipase B catalysed generation of peracid from a carboxylic acid is followed by a Prileshajev epoxidation of the corresponding allyl ether. Trimethylolpropane monoallyl ether (TMPME) was used as a model substrate. A maximal epoxide product yield of 77% was achieved through the optimization of temperature. acid concentration and hydrogen peroxide concentration. Peracid formation was considerably faster than the subsequent epoxidation step, and accumulation of the peracid was Found to be important to drive the epoxidation forward. (C) 2008 Elsevier B.V. All rights reserved. |
format | Article in Journal/Newspaper |
genre | Antarc* Antarctica |
genre_facet | Antarc* Antarctica |
id | ftulundlup:oai:lup.lub.lu.se:19d07118-98c0-414a-9a3a-e4958af8a624 |
institution | Open Polar |
language | English |
op_collection_id | ftulundlup |
op_container_end_page | 6 |
op_doi | https://doi.org/10.1016/j.molcatb.2007.11.015 |
op_relation | https://lup.lub.lu.se/record/1254666 http://dx.doi.org/10.1016/j.molcatb.2007.11.015 https://portal.research.lu.se/files/2825436/1268339.pdf wos:000257590000001 scopus:44649189738 |
op_rights | info:eu-repo/semantics/openAccess |
op_source | Journal of Molecular Catalysis B: Enzymatic; 54(1-2), pp 1-6 (2008) ISSN: 1873-3158 |
publishDate | 2008 |
publisher | Elsevier |
record_format | openpolar |
spelling | ftulundlup:oai:lup.lub.lu.se:19d07118-98c0-414a-9a3a-e4958af8a624 2025-04-06T14:34:02+00:00 Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers Tufvesson, Pär Adlercreutz, Dietlind Lundmark, Stefan Manea, Mircea Hatti-Kaul, Rajni 2008 application/pdf https://lup.lub.lu.se/record/1254666 https://doi.org/10.1016/j.molcatb.2007.11.015 https://portal.research.lu.se/files/2825436/1268339.pdf eng eng Elsevier https://lup.lub.lu.se/record/1254666 http://dx.doi.org/10.1016/j.molcatb.2007.11.015 https://portal.research.lu.se/files/2825436/1268339.pdf wos:000257590000001 scopus:44649189738 info:eu-repo/semantics/openAccess Journal of Molecular Catalysis B: Enzymatic; 54(1-2), pp 1-6 (2008) ISSN: 1873-3158 Industrial Biotechnology lipase allyl ether epoxidation glycidyl ether peracid contributiontojournal/article info:eu-repo/semantics/article text 2008 ftulundlup https://doi.org/10.1016/j.molcatb.2007.11.015 2025-03-11T14:07:53Z Production of glycidyl ethers is industrially carried Out by reacting alcohols with epichlorhydrin, a potentially carcinogenic compound. This paper investigates a less hazardous alternative-that of a chemo-enzymatic process in which Candida antarctica lipase B catalysed generation of peracid from a carboxylic acid is followed by a Prileshajev epoxidation of the corresponding allyl ether. Trimethylolpropane monoallyl ether (TMPME) was used as a model substrate. A maximal epoxide product yield of 77% was achieved through the optimization of temperature. acid concentration and hydrogen peroxide concentration. Peracid formation was considerably faster than the subsequent epoxidation step, and accumulation of the peracid was Found to be important to drive the epoxidation forward. (C) 2008 Elsevier B.V. All rights reserved. Article in Journal/Newspaper Antarc* Antarctica Lund University Publications (LUP) Journal of Molecular Catalysis B: Enzymatic 54 1-2 1 6 |
spellingShingle | Industrial Biotechnology lipase allyl ether epoxidation glycidyl ether peracid Tufvesson, Pär Adlercreutz, Dietlind Lundmark, Stefan Manea, Mircea Hatti-Kaul, Rajni Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title | Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title_full | Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title_fullStr | Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title_full_unstemmed | Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title_short | Production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
title_sort | production of glycidyl ethers by chemo-enzymatic epoxidation of allyl ethers |
topic | Industrial Biotechnology lipase allyl ether epoxidation glycidyl ether peracid |
topic_facet | Industrial Biotechnology lipase allyl ether epoxidation glycidyl ether peracid |
url | https://lup.lub.lu.se/record/1254666 https://doi.org/10.1016/j.molcatb.2007.11.015 https://portal.research.lu.se/files/2825436/1268339.pdf |