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Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles

Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alt...

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Autores principales: Betke, Tobias, Maier, Manuel, Gruber-Wölfler, Heidrun, Gröger, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269433/
https://www.ncbi.nlm.nih.gov/pubmed/30504854
http://dx.doi.org/10.1038/s41467-018-07434-0
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author Betke, Tobias
Maier, Manuel
Gruber-Wölfler, Heidrun
Gröger, Harald
author_facet Betke, Tobias
Maier, Manuel
Gruber-Wölfler, Heidrun
Gröger, Harald
author_sort Betke, Tobias
collection PubMed
description Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alternative approach towards such linear dinitriles is presented based on dehydration of readily available α,ω-dialdoximes at ambient conditions by means of aldoxime dehydratases. In contrast to existing production routes this biocatalytic route enables a highly regio- and chemoselective approach towards dinitriles without the use of hydrogen cyanide or harsh reaction conditions. In addition, a selective synthesis of adiponitrile with substrate loadings of up to 100 g/L and high yields of up to 80% was achieved. Furthermore, a lab scale process on liter scale leading to > 99% conversion at 50 g/L underlines the potential and robustness of this method for technical applicability.
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spelling pubmed-62694332018-12-03 Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles Betke, Tobias Maier, Manuel Gruber-Wölfler, Heidrun Gröger, Harald Nat Commun Article Linear α,ω-dinitriles are important precursors for the polymer industry. Most prominently, adiponitrile is produced on an annual scale of ca. 1 million tons. However, a drawback of today’s dominating process is the need for large amounts of highly toxic hydrogen cyanide. In this contribution, an alternative approach towards such linear dinitriles is presented based on dehydration of readily available α,ω-dialdoximes at ambient conditions by means of aldoxime dehydratases. In contrast to existing production routes this biocatalytic route enables a highly regio- and chemoselective approach towards dinitriles without the use of hydrogen cyanide or harsh reaction conditions. In addition, a selective synthesis of adiponitrile with substrate loadings of up to 100 g/L and high yields of up to 80% was achieved. Furthermore, a lab scale process on liter scale leading to > 99% conversion at 50 g/L underlines the potential and robustness of this method for technical applicability. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269433/ /pubmed/30504854 http://dx.doi.org/10.1038/s41467-018-07434-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Betke, Tobias
Maier, Manuel
Gruber-Wölfler, Heidrun
Gröger, Harald
Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title_full Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title_fullStr Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title_full_unstemmed Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title_short Biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
title_sort biocatalytic production of adiponitrile and related aliphatic linear α,ω-dinitriles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269433/
https://www.ncbi.nlm.nih.gov/pubmed/30504854
http://dx.doi.org/10.1038/s41467-018-07434-0
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