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Chromium‐Catalyzed Alkylation of Amines by Alcohols

The alkylation of amines by alcohols is a broadly applicable, sustainable, and selective method for the synthesis of alkyl amines, which are important bulk and fine chemicals, pharmaceuticals, and agrochemicals. We show that Cr complexes can catalyze this C−N bond formation reaction. We synthesized...

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Autores principales: Kallmeier, Fabian, Fertig, Robin, Irrgang, Torsten, Kempe, Rhett
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384194/
https://www.ncbi.nlm.nih.gov/pubmed/32187785
http://dx.doi.org/10.1002/anie.202001704
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author Kallmeier, Fabian
Fertig, Robin
Irrgang, Torsten
Kempe, Rhett
author_facet Kallmeier, Fabian
Fertig, Robin
Irrgang, Torsten
Kempe, Rhett
author_sort Kallmeier, Fabian
collection PubMed
description The alkylation of amines by alcohols is a broadly applicable, sustainable, and selective method for the synthesis of alkyl amines, which are important bulk and fine chemicals, pharmaceuticals, and agrochemicals. We show that Cr complexes can catalyze this C−N bond formation reaction. We synthesized and isolated 35 examples of alkylated amines, including 13 previously undisclosed products, and the use of amino alcohols as alkylating agents was demonstrated. The catalyst tolerates numerous functional groups, including hydrogenation‐sensitive examples. Compared to many other alcohol‐based amine alkylation methods, where a stoichiometric amount of base is required, our Cr‐based catalyst system gives yields higher than 90 % for various alkyl amines with a catalytic amount of base. Our study indicates that Cr complexes can catalyze borrowing hydrogen or hydrogen autotransfer reactions and could thus be an alternative to Fe, Co, and Mn, or noble metals in (de)hydrogenation catalysis.
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spelling pubmed-73841942020-07-28 Chromium‐Catalyzed Alkylation of Amines by Alcohols Kallmeier, Fabian Fertig, Robin Irrgang, Torsten Kempe, Rhett Angew Chem Int Ed Engl Communications The alkylation of amines by alcohols is a broadly applicable, sustainable, and selective method for the synthesis of alkyl amines, which are important bulk and fine chemicals, pharmaceuticals, and agrochemicals. We show that Cr complexes can catalyze this C−N bond formation reaction. We synthesized and isolated 35 examples of alkylated amines, including 13 previously undisclosed products, and the use of amino alcohols as alkylating agents was demonstrated. The catalyst tolerates numerous functional groups, including hydrogenation‐sensitive examples. Compared to many other alcohol‐based amine alkylation methods, where a stoichiometric amount of base is required, our Cr‐based catalyst system gives yields higher than 90 % for various alkyl amines with a catalytic amount of base. Our study indicates that Cr complexes can catalyze borrowing hydrogen or hydrogen autotransfer reactions and could thus be an alternative to Fe, Co, and Mn, or noble metals in (de)hydrogenation catalysis. John Wiley and Sons Inc. 2020-05-18 2020-07-13 /pmc/articles/PMC7384194/ /pubmed/32187785 http://dx.doi.org/10.1002/anie.202001704 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Kallmeier, Fabian
Fertig, Robin
Irrgang, Torsten
Kempe, Rhett
Chromium‐Catalyzed Alkylation of Amines by Alcohols
title Chromium‐Catalyzed Alkylation of Amines by Alcohols
title_full Chromium‐Catalyzed Alkylation of Amines by Alcohols
title_fullStr Chromium‐Catalyzed Alkylation of Amines by Alcohols
title_full_unstemmed Chromium‐Catalyzed Alkylation of Amines by Alcohols
title_short Chromium‐Catalyzed Alkylation of Amines by Alcohols
title_sort chromium‐catalyzed alkylation of amines by alcohols
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7384194/
https://www.ncbi.nlm.nih.gov/pubmed/32187785
http://dx.doi.org/10.1002/anie.202001704
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