Nitrile hydration provides access to amides that are important structural elements in organic chemistry. Here we report catalytic nitrile hydration using ruthenium catalysts based on a pincer scaffold with a dearomatized pyridine backbone. These complexes catalyze the nucleophilic addition of HO to a wide variety of aliphatic and (hetero)aromatic nitriles in BuOH as solvent. Reactions occur under mild conditions (room temperature) in the absence of additives. A mechanism for nitrile hydration is proposed that is initiated by metal-ligand cooperative binding of the nitrile.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7020783 | PMC |
http://dx.doi.org/10.1039/c9sc04624k | DOI Listing |
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