Reactions of Malononitrile with Cross-conjugated Dienone Derivatives of Cyclohexane. Synthesis of Substituted Partially Hydrogenated Quinoline- and Chromenecarbonitriles


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The condensation of malononitrile with unsymmetrical dienones of the cyclohexane series under basic conditions selectively afforded substituted tetrahydroquinolinecarbonitriles. The reaction of 2,6-bis-(3-nitrophenylmethylidene)cyclohexan-1-one with malononitrile under similar conditions led to the formation of substituted tetrahydrochromenecarbonitrile. Factors determining the reaction direction and selectivity were discussed. The structure of the newly synthesized compounds was confirmed by IR and 1H NMR spectra.

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N. Vasilkova

Institute of Chemistry; Institute of Chemistry

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Email: vasilkovano@mail.ru
俄罗斯联邦, Saratov; Saratov

A. Kalugina

Institute of Chemistry

Email: vasilkovano@mail.ru
俄罗斯联邦, Saratov

A. Nikulin

Institute of Chemistry

Email: vasilkovano@mail.ru
俄罗斯联邦, Saratov

A. Krivenko

Institute of Chemistry

Email: vasilkovano@mail.ru
俄罗斯联邦, Saratov

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