Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence
Abstract A sequential, chemoenzymatic process for a continuously operating production of the chiral β‐amino acid ester ethyl ( S )‐3‐(benzylamino)butanoate was developed. The reactor set‐up combined a plug‐flow reactor for the thermal aza‐Michael addition of benzylamine to trans ‐ethyl crotonate cou...
Published in: | Advanced Synthesis & Catalysis |
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crwiley:10.1002/adsc.201300236 2024-06-23T07:45:50+00:00 Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence Strompen, Simon Weiß, Markus Gröger, Harald Hilterhaus, Lutz Liese, Andreas 2013 http://dx.doi.org/10.1002/adsc.201300236 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadsc.201300236 https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201300236 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Advanced Synthesis & Catalysis volume 355, issue 11-12, page 2391-2399 ISSN 1615-4150 1615-4169 journal-article 2013 crwiley https://doi.org/10.1002/adsc.201300236 2024-06-11T04:49:28Z Abstract A sequential, chemoenzymatic process for a continuously operating production of the chiral β‐amino acid ester ethyl ( S )‐3‐(benzylamino)butanoate was developed. The reactor set‐up combined a plug‐flow reactor for the thermal aza‐Michael addition of benzylamine to trans ‐ethyl crotonate coupled to a subsequent packed‐bed reactor for the lipase (Novozym 435)‐catalyzed kinetic resolution of the racemic intermediate product, which was formed in the initial step. The coupled reactors were operated continuously for a time period of 4 days without significant loss of enzyme activity. The target β‐amino acid ester was obtained with 92% conversion in the plug‐flow reactor and 59% conversion in the packed bed reactor at high enantiomeric excess of >98%. A space‐time yield of 0.4 kg L −1 d −1 was calculated for the total reactor system and 1.8 kg L −1 d −1 based solely on the volume of the packed bed reactor. A total turnover number of 158,000 was calculated for the biocatalyst assuming the same deactivation rate as observed in batch experiments. The continuously operating, solvent‐free process thus represents an efficient method for the enantioselective production of a value added ( S )‐β‐amino acid ester starting from cheap substrates. Abbreviations: CALB= Candida antarctica lipase B; CSTR=continuously stirred tank reactor; d i =inner diameter [mm]; ee =enantiomeric excess; ε =porosity; k cat,obs =apparent turnover number [h −1 ]; k deact =enzyme deactivation constant [h −1 ]; L=length of reactor [m]; m̄ p =average mass of a single particle [g]; N435=Novozym 435 ( Candida antarctica lipase B immobilized on acrylic resin); PBR=packed‐bed reactor; PFR=plug‐flow reactor; PTFE=polytetrafluoroethylene; ρ bp =bulk particle density [kg m −3 ]; ρ p =density of carrier material [kg m −3 ]; Q=productivity [kg ${{\rm kg}{{- 1\hfill \atop {\rm N435}\hfill}}}$ d −1 ]; R=channel radius of curvature [cm]; ttn= total turnover number [mol mol −1 ]; T=temperature [°C]; τ =residence time [h]; u f =fluid velocity [cm min −1 ]; ... Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Advanced Synthesis & Catalysis 355 11-12 2391 2399 |
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Wiley Online Library |
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English |
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Abstract A sequential, chemoenzymatic process for a continuously operating production of the chiral β‐amino acid ester ethyl ( S )‐3‐(benzylamino)butanoate was developed. The reactor set‐up combined a plug‐flow reactor for the thermal aza‐Michael addition of benzylamine to trans ‐ethyl crotonate coupled to a subsequent packed‐bed reactor for the lipase (Novozym 435)‐catalyzed kinetic resolution of the racemic intermediate product, which was formed in the initial step. The coupled reactors were operated continuously for a time period of 4 days without significant loss of enzyme activity. The target β‐amino acid ester was obtained with 92% conversion in the plug‐flow reactor and 59% conversion in the packed bed reactor at high enantiomeric excess of >98%. A space‐time yield of 0.4 kg L −1 d −1 was calculated for the total reactor system and 1.8 kg L −1 d −1 based solely on the volume of the packed bed reactor. A total turnover number of 158,000 was calculated for the biocatalyst assuming the same deactivation rate as observed in batch experiments. The continuously operating, solvent‐free process thus represents an efficient method for the enantioselective production of a value added ( S )‐β‐amino acid ester starting from cheap substrates. Abbreviations: CALB= Candida antarctica lipase B; CSTR=continuously stirred tank reactor; d i =inner diameter [mm]; ee =enantiomeric excess; ε =porosity; k cat,obs =apparent turnover number [h −1 ]; k deact =enzyme deactivation constant [h −1 ]; L=length of reactor [m]; m̄ p =average mass of a single particle [g]; N435=Novozym 435 ( Candida antarctica lipase B immobilized on acrylic resin); PBR=packed‐bed reactor; PFR=plug‐flow reactor; PTFE=polytetrafluoroethylene; ρ bp =bulk particle density [kg m −3 ]; ρ p =density of carrier material [kg m −3 ]; Q=productivity [kg ${{\rm kg}{{- 1\hfill \atop {\rm N435}\hfill}}}$ d −1 ]; R=channel radius of curvature [cm]; ttn= total turnover number [mol mol −1 ]; T=temperature [°C]; τ =residence time [h]; u f =fluid velocity [cm min −1 ]; ... |
format |
Article in Journal/Newspaper |
author |
Strompen, Simon Weiß, Markus Gröger, Harald Hilterhaus, Lutz Liese, Andreas |
spellingShingle |
Strompen, Simon Weiß, Markus Gröger, Harald Hilterhaus, Lutz Liese, Andreas Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
author_facet |
Strompen, Simon Weiß, Markus Gröger, Harald Hilterhaus, Lutz Liese, Andreas |
author_sort |
Strompen, Simon |
title |
Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
title_short |
Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
title_full |
Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
title_fullStr |
Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
title_full_unstemmed |
Development of a Continuously Operating Process for the Enantioselective Synthesis of a β‐Amino Acid Ester via a Solvent‐Free Chemoenzymatic Reaction Sequence |
title_sort |
development of a continuously operating process for the enantioselective synthesis of a β‐amino acid ester via a solvent‐free chemoenzymatic reaction sequence |
publisher |
Wiley |
publishDate |
2013 |
url |
http://dx.doi.org/10.1002/adsc.201300236 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fadsc.201300236 https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201300236 |
genre |
Antarc* Antarctica |
genre_facet |
Antarc* Antarctica |
op_source |
Advanced Synthesis & Catalysis volume 355, issue 11-12, page 2391-2399 ISSN 1615-4150 1615-4169 |
op_rights |
http://onlinelibrary.wiley.com/termsAndConditions#vor |
op_doi |
https://doi.org/10.1002/adsc.201300236 |
container_title |
Advanced Synthesis & Catalysis |
container_volume |
355 |
container_issue |
11-12 |
container_start_page |
2391 |
op_container_end_page |
2399 |
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1802642613729230848 |