DEDIAZONIATION REACTIONS OF ARENEDIAZONIUM IONS UNDER SOLVOLYTIC CONDITIONS - FLUORIDE ANION ABSTRACTION FROM TRIFLUOROETHANOL AND ALPHA-HYDROGEN ATOM ABSTRACTION FROM ETHANOL
Psj. Canning et al., DEDIAZONIATION REACTIONS OF ARENEDIAZONIUM IONS UNDER SOLVOLYTIC CONDITIONS - FLUORIDE ANION ABSTRACTION FROM TRIFLUOROETHANOL AND ALPHA-HYDROGEN ATOM ABSTRACTION FROM ETHANOL, Chemical communications, (18), 1998, pp. 1971-1972
Arenediazonium salts decompose thermally and photochemically in triflu
oroethanol to yield trifluoroethyl ethers and (in part by fluoride abs
traction from the solvent) fluoroarenes; the less reactive compounds i
n trifluoroethanol decompose readily in ethanol to give arenes in a ra
dical reaction involving abstraction of the ct-hydrogen from the ethan
ol.