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Reactions of 2,2-disubstituted 1,1-dicyanoethenes with β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-trimethoxypropane

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Abstract

A reaction of 2,2-disubstituted 1,1-dicyanoethenes with β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-trimethoxypropane leads to substituted 6,6-dicyano-1-dimethyl-aminohexatrienes and an organic salt containing 1,1,9,9-tetracyano-2,8-diphenylnona-2,4,6,8-tetraenide as the anion and (dimethylaminopropenylidene)dimethylammonium as the cation, on the basis of which new cation-anionic polymethine dyes were obtained.

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Authors and Affiliations

  1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

    Zh. A. Krasnaya, E. O. Tret’yakova, V. V. Kachala & S. G. Zlotin

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  1. Zh. A. Krasnaya
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  2. E. O. Tret’yakova
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  3. V. V. Kachala
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  4. S. G. Zlotin
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Correspondence to Zh. A. Krasnaya.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1639–1643, August, 2008.

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Krasnaya, Z.A., Tret’yakova, E.O., Kachala, V.V. et al. Reactions of 2,2-disubstituted 1,1-dicyanoethenes with β-dimethylaminoacrolein aminal and 3-dimethylamino-1,1,3-trimethoxypropane. Russ Chem Bull 57, 1671–1675 (2008). https://doi.org/10.1007/s11172-008-0219-0

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  • DOI: https://doi.org/10.1007/s11172-008-0219-0

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