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Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine

Candida antarctica lipase B (CALB) and racemization catalyst 4 were combined in the dynamic kinetic resolution (DKR) of (±)-1-phenylethylamine (1). Several reaction parameters have been investigated to modify the method for application on multigram scale. A comparison of isopropyl acetate and alkyl...

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Autores principales: Thalén, Lisa K, Bäckvall, Jan-E
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956483/
https://www.ncbi.nlm.nih.gov/pubmed/20978623
http://dx.doi.org/10.3762/bjoc.6.97
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author Thalén, Lisa K
Bäckvall, Jan-E
author_facet Thalén, Lisa K
Bäckvall, Jan-E
author_sort Thalén, Lisa K
collection PubMed
description Candida antarctica lipase B (CALB) and racemization catalyst 4 were combined in the dynamic kinetic resolution (DKR) of (±)-1-phenylethylamine (1). Several reaction parameters have been investigated to modify the method for application on multigram scale. A comparison of isopropyl acetate and alkyl methoxyacetates as acyl donors was carried out. It was found that lower catalyst loadings could be used to obtain (R)-2-methoxy-N-(1-phenylethyl)acetamide (3) in good yield and high ee when alkyl methoxyacetates were used as acyl donors compared to when isopropyl acetate was used as the acyl donor. The catalyst loading could be decreased to 1.25 mol % Ru-catalyst 4 and 10 mg CALB per mmol 1 when alkyl methoxyacetates were used as the acyl donor.
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spelling pubmed-29564832010-10-26 Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine Thalén, Lisa K Bäckvall, Jan-E Beilstein J Org Chem Full Research Paper Candida antarctica lipase B (CALB) and racemization catalyst 4 were combined in the dynamic kinetic resolution (DKR) of (±)-1-phenylethylamine (1). Several reaction parameters have been investigated to modify the method for application on multigram scale. A comparison of isopropyl acetate and alkyl methoxyacetates as acyl donors was carried out. It was found that lower catalyst loadings could be used to obtain (R)-2-methoxy-N-(1-phenylethyl)acetamide (3) in good yield and high ee when alkyl methoxyacetates were used as acyl donors compared to when isopropyl acetate was used as the acyl donor. The catalyst loading could be decreased to 1.25 mol % Ru-catalyst 4 and 10 mg CALB per mmol 1 when alkyl methoxyacetates were used as the acyl donor. Beilstein-Institut 2010-09-13 /pmc/articles/PMC2956483/ /pubmed/20978623 http://dx.doi.org/10.3762/bjoc.6.97 Text en Copyright © 2010, Thalén and Bäckvall https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Thalén, Lisa K
Bäckvall, Jan-E
Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title_full Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title_fullStr Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title_full_unstemmed Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title_short Development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
title_sort development of dynamic kinetic resolution on large scale for (±)-1-phenylethylamine
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956483/
https://www.ncbi.nlm.nih.gov/pubmed/20978623
http://dx.doi.org/10.3762/bjoc.6.97
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