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Structure of Products of Reaction between Benzoylacetylene and 1,5-Diphenyldithiobiuret.

Authors :
Glotova, T.
Nakhmanovich, A.
Albanov, A.
Protsuk, N.
Nizovtseva, T.
Lopyrev, V.
Source :
Chemistry of Heterocyclic Compounds; Jan2002, Vol. 38 Issue 1, p74-78, 5p
Publication Year :
2002

Abstract

Reaction of benzoylacetylene with 1,5-diphenyldithiobiuret in glacial AcOH in the presence of equimolar amounts of HClO<subscript>4</subscript> leads exclusively to 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazinium perchlorate. In MeOH, benzene, and MeCN medium, the reaction proceeds nonselectively and a mixture is formed that includes 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazine, 2-benzoylmethyl-4-benzoylvinylthio-3-phenyl-6-phenylimino-1,3,5-thiadiazine, 2-benzoylmethyl-4,6-di-(thiocarbonyl)-1,3-diphenyl-1,3,5-triazine, and N-benzoylvinyl-N'-phenylthiourea. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00093122
Volume :
38
Issue :
1
Database :
Complementary Index
Journal :
Chemistry of Heterocyclic Compounds
Publication Type :
Academic Journal
Accession number :
49910456
Full Text :
https://doi.org/10.1023/A:1014859410679