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Synthesis and some reactions of phosphorylated derivatives of s-triazine

Journal Article · · J. Gen. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:5793803
Tris(dialkoxyphosphinothioylthio)-s-triazines show no tendency to undergo tautomeric processes. When heated, they are converted into 0,0-dialkyl phosphorisothiocyanatidothioates. In the treatment of tris(dialkoxyphosphinothioylthio)-s-triazines with aniline the replacement of the dialkoxyphosphinothioylthio groups occurs with the formation of (dianilino-s-triazinyl)-phenylammonium 0,0-dialkyl phosphorodithioates. The reactions with 0,0-dialkyl hydrogen phosphorodithioates lead to the formation of tetraalkyl trithiopyrophosphoates. Tris(dialkoxyphosphinylthio)-s-triazines are capable of tautomerism, arising from the S in equilibrium N migration of phosphoryl groups. The tautomerization goes intermolecularly and stagewise. Tris(dialkoxyphosphinylthio)-s-triazines undergo hydrolysis under mild conditions, leading finally to the formation of 1-(dialkoxyphosphinyl)tetrahydro-4,6-dithioxo-s-traizin-2(1H)-ones.
Research Organization:
V.I. Ul'yanov-Lenin Kazan' State Univ., USSR
OSTI ID:
5793803
Journal Information:
J. Gen. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Gen. Chem. USSR (Engl. Transl.); (United States) Vol. 55:12; ISSN JGCHA
Country of Publication:
United States
Language:
English