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Reaction of divinyl ether with phosphorus pentachloride

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5025147
It is known that divinyl sulfides are phosphorylated by phosphorus pentachloride with the formation of 1,4-thiaphosphorin derivatives. The authors have found that divinyl ether is phosphorylated by phosphorus pentachloride in a benzene medium with the formation of 4,4-dichloro-4H-1,4-oxaphosphorin-4-ium hexachlorophosphate; the process goes analogously to the phosphorylation of divinyl sulfide. The /sup 1/H, /sup 31/P, and /sup 13/C NMR spectra were recorded on a Bruker WP-200SY spectrometer at room temperature. Stabilization was effected by the signal of deuterium in CDCl/sub 3/. The /sup 31/P signals were recorded relative to 85% H/sub 3/PO/sub 4/ as external standard.
Research Organization:
A. A. Zhdanov Irkut-sk State Univ. (USSR)
OSTI ID:
5025147
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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