The Feist-Benary synthesis is a chemical reaction of α-halogen ketones and β-dicarbonyl compounds to give substituted furan compounds.This condensation reaction is catalyzed by amines like ammonia and pyridine. The initial step in the ring synthesis is associated to the Knoevenagel condensation. In the second step the enolate shifts an alkyl halogen in a nucleophilic aliphatic substitution.
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