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...

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Published in:Journal of Molecular Catalysis B: Enzymatic
Main Authors: Tufvesson, Pär, Adlercreutz, Dietlind, Lundmark, Stefan, Manea, Mircea, Hatti-Kaul, Rajni
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2008
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.
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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
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op_source Journal of Molecular Catalysis B: Enzymatic; 54(1-2), pp 1-6 (2008)
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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