Paper
2,3,5,6-Tetra(vinylthio)difluorobenzene in Reactions with Difunctional Nucleophiles
Published Dec 1, 2001 · V. I. Gostevskaya, G. M. Gavrilova, A. Afonin
Russian Journal of Organic Chemistry
3
Citations
0
Influential Citations
Abstract
Reaction of 2,3,5,6-tetra(vinylthio)difluorobenzene with ethylene glycol affords 1,4-bis[2,3,5,6-tetra(vinylthio)-4-fluorophenoxy-1-ethyloxy-]-2,3,5,6-tetra(vinylthio)benzene, with diethylene glycol arises 2,3,5,6-tetra(vinylthio)-4-(4-hydroxyethoxyethyloxy)-1-fluorobenzene, with 1,5-diaminopentane forms 1,5-bis[2,3,5,6-tetra(vinylthio)-4-fluoroanilino]pentane; in reactions with 2-aminoethanethiol and 2-mercaptoethanol occurs substitution of two fluorine atoms by RS groups.
This study demonstrates that 2,3,5,6-tetra(vinylthio)difluorobenzene can form complex compounds with difunctional nucleophiles, resulting in fluorine substitution and RS group substitution.
Full text analysis coming soon...