Abstract
The reaction of benzylidene hydrazines (1) with various haloacyl halides (2) was carried out in aqueous NaOH-CH2Cl2 in the presence of a phase transfer catalyst to afford 1, 4-(diphenylmethyleneamino) piperazine-2, 5-diones (3) and N-phenylmethyleneamino-β, γ, and δ-lactams in yields of 31-84%.