Synthesis of carbonyl compounds based on the products of addition of polyhaloalkanes to unsaturated systems. Reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate |
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Authors: | S A Woznesensky A A Dudinov L I Belen'kii M I Struchkova V N Nesterov M M Krayushkin Yu T Struchkov |
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Institution: | (1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913 Moscow, Russian Federation;(2) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation |
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Abstract: | The reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate in the presence of EtONa give ethyl 4-aryl-6-(2,2-dichlorovinyl)-4-hydroxy-2-oxocyclohexane-carboxylates.
The structures of the reaction products were confirmed by1H and13C NMR spectroscopy and by X-ray diffraction analysis.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. |
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Keywords: | ethyl 4-aryl-6-(2 2-dichlorovinyl)-4-hydroxy-2-oxocyclohexanecarboxylates synthesis 1-aryl-5 5-dichloropenta-2 4-dien-1-ones ethyl acetoacetate condensation cyclization crystal structure 1H and13C NMR spectra |
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