Ruthenium-catalyzed deaminative hydrogenation of aliphatic and aromatic nitriles to primary alcohols

The deaminative hydrogenation of nitriles towards alcohols is a useful reaction to transform nitriles into alcohols with NH3 as the sole byproduct. Using the simple and robust RuHCl(CO)(PPh3)3 complex as a catalyst, at low H2 pressures a series of aliphatic and aromatic nitriles could be transformed...

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Bibliographic Details
Main Authors: Molnár, István G. (Author) , Calleja Ramos, Pilar (Author) , Hashmi, A. Stephen K. (Author) , Schaub, Thomas (Author)
Format: Article (Journal)
Language:English
Published: 4 July 2017
In: ChemCatChem
Year: 2017, Volume: 9, Issue: 22, Pages: 4175-4178
ISSN:1867-3899
DOI:10.1002/cctc.201700878
Online Access:Verlag, Volltext: http://dx.doi.org/10.1002/cctc.201700878
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/cctc.201700878
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Author Notes:István Gábor Molnár, Pilar Calleja, Martin Ernst, A. Stephen K. Hashmi, Thomas Schaub
Description
Summary:The deaminative hydrogenation of nitriles towards alcohols is a useful reaction to transform nitriles into alcohols with NH3 as the sole byproduct. Using the simple and robust RuHCl(CO)(PPh3)3 complex as a catalyst, at low H2 pressures a series of aliphatic and aromatic nitriles could be transformed into the corresponding alcohols. Suitable solvent systems for these reactions were 1,4-dioxane/water and EtOH/water mixtures. In most cases, the selectivity for the alcohols was excellent, and the corresponding amines were formed only in trace amounts.
Item Description:Gesehen am 25.04.2018
Physical Description:Online Resource
ISSN:1867-3899
DOI:10.1002/cctc.201700878