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Phosphorylation of halogen-substituted. beta. -dicarbonyl compounds with phosphorus chloride in presence of triethylamine

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5129273

We studied the reactions of polyfluorinated ..beta..-dicarbonyl groups with phosphorus(III) chlorides in presence of triethylamine. In the reactions of the phosphorochloridites with 4,4,4-trifluoroacetoacetic ester and its chloro derivative we obtained some new vinyl phosphites with two and three electron-acceptor substituents in the vinyl group. The structures of the compounds are confirmed by their IR and /sup 1/H and /sup 31/P NMR spectra. The PMR data show that the phosphorylation of 4,4,4-trifluoroacetoacetic ester (unlike unsubstituted acetoacetic ester) goes stereo-selectively.

Research Organization:
Institute of Organic Chemistry, Kiev (USSR)
OSTI ID:
5129273
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 57:4; ISSN JGCHA
Country of Publication:
United States
Language:
English

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