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Hydration of nitriles using a metal-ligand cooperative ruthenium pincer catalyst.

Beibei GuoJohannes G de VriesEdwin Otten
Published in: Chemical science (2019)
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 t 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.
Keyphrases
  • room temperature
  • ionic liquid
  • highly efficient
  • transcription factor
  • binding protein
  • tissue engineering
  • transition metal
  • water soluble
  • carbon dioxide