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 H2O to a wide variety of aliphatic and (hetero)aromatic nitriles in tBuOH 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.
CITATION STYLE
Guo, B., & De Vries, J. G. (2019). Hydration of nitriles using a metal-ligand cooperative ruthenium pincer catalyst. Chemical Science, 10(45), 10647–10652. https://doi.org/10.1039/c9sc04624k
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