Organocatalytic conjugate addition of 1-bromonitroalkanes to α,β-unsaturated aldehydes: synthesis of nitrocyclopropanes

A variety of secondary amines were studied as the catalyst in the conjugate addition of 1-bromonitromethane to α,β-unsaturated aldehydes. Proline was identified as the best catalyst for this reaction. MeOH/AcONa system was found to provide much better yields than CHCl3/Et3N system reported before. Good yields of nitrocyclopropane products were obtained with a variety of β-aryl acroleins. Several substituted 1-bromonitromethanes were also examined in the reaction. Both 1-bromonitroethane and 1-phenyl-1-bromonitromethane gave the corresponding nitrocyclopropanes in good yields. The diastereoselectivity of the reaction was strongly affected by the steric hindrance of 1-bromonitroalkanes.

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