Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.

Fatty alcohols are important products in chemical industry to be used in the formulation of surfactants and lubricants. This work describes a two step approach for the production of myristyl alcohol under neat conditions by combining a lipase catalyzed esterification of myristic acid and myristyl al...

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Published in:Organic & Biomolecular Chemistry
Main Authors: Schlipköter, Kim E, Betke, Tobias, Kleber, Joscha, Gröger, Harald, Liese, Andreas
Format: Article in Journal/Newspaper
Language:English
Published: Royal Society of Chemistry 2020
Subjects:
Online Access:https://doi.org/10.1039/d0ob01561j
https://pubmed.ncbi.nlm.nih.gov/32975273
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spelling ftpubmed:32975273 2024-09-15T17:44:48+00:00 Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation. Schlipköter, Kim E Betke, Tobias Kleber, Joscha Gröger, Harald Liese, Andreas 2020 Oct 14 https://doi.org/10.1039/d0ob01561j https://pubmed.ncbi.nlm.nih.gov/32975273 eng eng Royal Society of Chemistry https://doi.org/10.1039/d0ob01561j https://pubmed.ncbi.nlm.nih.gov/32975273 Org Biomol Chem ISSN:1477-0539 Volume:18 Issue:39 Journal Article 2020 ftpubmed https://doi.org/10.1039/d0ob01561j 2024-07-25T16:05:00Z Fatty alcohols are important products in chemical industry to be used in the formulation of surfactants and lubricants. This work describes a two step approach for the production of myristyl alcohol under neat conditions by combining a lipase catalyzed esterification of myristic acid and myristyl alcohol with a ruthenium catalyzed hydrogenation of the intermediate myristyl myristate. The esterification was carried out in a bubble column reactor with the commercial immobilized lipase B from Candida antarctica as a biocatalyst, while the hydrogenation was conducted under pressurized conditions being catalyzed by the homogeneous chemocatalyst Ru-Macho-BH. By investigating the reaction steps separately, comparable reaction rates were found for the esterification of short chain and long chain alcohols. Additionally, the hydrogen pressure could be reduced to 35 bar compared to the current industrial Lurgi process. Characterization of cross interactions by the reactants myristic acid and sodium myristate in the hydrogenation demonstrates that the metal catalyst was completely deactivated, even at a low amount of 0.5 mol% of myristic acid. Complete conversion of myristic acid in the esterification with equal amounts of myristic acid and myristyl alcohol was obtained, overcoming any limitation in the hydrogenation. In comparison to the Lurgi process starting also from fatty acid and fatty alcohols, the chemoenzymatic two step reaction sequence could be realized at lower reaction temperatures of 60 and 100 °C as well as lower hydrogen pressures of 35 bar. Article in Journal/Newspaper Antarc* Antarctica PubMed Central (PMC) Organic & Biomolecular Chemistry 18 39 7862 7867
institution Open Polar
collection PubMed Central (PMC)
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language English
description Fatty alcohols are important products in chemical industry to be used in the formulation of surfactants and lubricants. This work describes a two step approach for the production of myristyl alcohol under neat conditions by combining a lipase catalyzed esterification of myristic acid and myristyl alcohol with a ruthenium catalyzed hydrogenation of the intermediate myristyl myristate. The esterification was carried out in a bubble column reactor with the commercial immobilized lipase B from Candida antarctica as a biocatalyst, while the hydrogenation was conducted under pressurized conditions being catalyzed by the homogeneous chemocatalyst Ru-Macho-BH. By investigating the reaction steps separately, comparable reaction rates were found for the esterification of short chain and long chain alcohols. Additionally, the hydrogen pressure could be reduced to 35 bar compared to the current industrial Lurgi process. Characterization of cross interactions by the reactants myristic acid and sodium myristate in the hydrogenation demonstrates that the metal catalyst was completely deactivated, even at a low amount of 0.5 mol% of myristic acid. Complete conversion of myristic acid in the esterification with equal amounts of myristic acid and myristyl alcohol was obtained, overcoming any limitation in the hydrogenation. In comparison to the Lurgi process starting also from fatty acid and fatty alcohols, the chemoenzymatic two step reaction sequence could be realized at lower reaction temperatures of 60 and 100 °C as well as lower hydrogen pressures of 35 bar.
format Article in Journal/Newspaper
author Schlipköter, Kim E
Betke, Tobias
Kleber, Joscha
Gröger, Harald
Liese, Andreas
spellingShingle Schlipköter, Kim E
Betke, Tobias
Kleber, Joscha
Gröger, Harald
Liese, Andreas
Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
author_facet Schlipköter, Kim E
Betke, Tobias
Kleber, Joscha
Gröger, Harald
Liese, Andreas
author_sort Schlipköter, Kim E
title Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
title_short Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
title_full Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
title_fullStr Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
title_full_unstemmed Fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
title_sort fatty alcohol synthesis from fatty acids at mild temperature by subsequent enzymatic esterification and metal-catalyzed hydrogenation.
publisher Royal Society of Chemistry
publishDate 2020
url https://doi.org/10.1039/d0ob01561j
https://pubmed.ncbi.nlm.nih.gov/32975273
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Org Biomol Chem
ISSN:1477-0539
Volume:18
Issue:39
op_relation https://doi.org/10.1039/d0ob01561j
https://pubmed.ncbi.nlm.nih.gov/32975273
op_doi https://doi.org/10.1039/d0ob01561j
container_title Organic & Biomolecular Chemistry
container_volume 18
container_issue 39
container_start_page 7862
op_container_end_page 7867
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