Home Chemistry Heterocyclic Building Blocks Pyridines 2-(Pyridin-3-Yl)Acetonitrile
Nucleophilic substitution reactions: The nitrile group can undergo nucleophilic substitution reactions with various nucleophiles, such as amines, alcohols, and thiols, to form corresponding amides, esters, and thioamides, respectively.
Grignard reactions: 2-(pyridin-3-yl)acetonitrile can react with Grignard reagents to form substituted pyridine derivatives.
Reduction reactions: The nitrile group can be reduced to primary amines using reducing agents such as lithium aluminum hydride (LiAlH4) or hydrogen gas in the presence of a catalyst (e.g., Raney nickel).
Cyanation reactions: The pyridine ring can undergo cyanation reactions to introduce additional nitrile groups at different positions on the ring.
Metal-catalyzed cross-coupling reactions: 2-(pyridin-3-yl)acetonitrile can participate in metal-catalyzed cross-coupling reactions, such as Suzuki, Heck, or Sonogashira coupling, to form biaryl or vinyl-substituted pyridine derivatives.
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