333800-18-3Relevant articles and documents
Zonov, Yaroslav V.,Karpov, Victor M.,Mezhenkova, Tatyana V.,Platonov, Vyacheslav E.
, p. 24 - 34 (2018/08/17)
Synthesis and skeletal rearrangements of perfluorinated 4-alkyl- and 4-phenyl-tetralin-1-ones under the action of antimony pentafluoride
Zonov, Yaroslav V.,Karpov, Victor M.,Platonov, Vyacheslav E.
, p. 159 - 166 (2012/04/10)
Heating of perfluorinated 1-methyl- and 1-ethyltetralins with SiO 2 in an SbF5 medium at 100 °C results in perfluoro-4-alkyltetralin-1-ones formation. Perfluoro-4-methyltetralin-1-one, under the action of SbF5 at 180 °C with subsequent treatment of the reaction mixture with water, is converted to perfluoro-3,3-dimethylindan-1- one and perfluoro-3,4-dimethylisochromen-1-one. Perfluoro-4-ethyltetralin-1-one, under similar conditions, forms perfluoro-3-ethyl-3-methylindan-1-one, perfluoro-4-ethyl-3-methylisochromen-1-one and perfluoro-2-methyltetralin. Reaction of perfluorotetralin-1-one with pentafluorobenzene in the presence of SbF5 at 50-55 °C leads to the formation of perfluoro-4- phenyltetralin-1-one, which under the action of SbF5 at 75 °C isomerizes into perfluoro-3-methyl-3-phenylindan-1-one. Heating of the latter with SbF5 at 75-95 °C gives, after treatment of the reaction mixture with water, perfluoro-2-(2-methylphenyl)-3-phenylpropenoic acid and perfluoro-4-methyl-3-phenylisochromen-1-one.
Skeletal transformations of perfluoro-1-phenylindan under the action of antimony pentafluoride
Karpov,Mezhenkova,Platonov,Sinyakov
, p. 53 - 57 (2007/10/03)
Perfluoro-1-phenylindan (1) was obtained from perfluoroindan and pentafluorobenzene in the presence of SbF5. Compound 1 heated with antimony pentafluoride at 170°C and then treated with water gave a mixture of perfluorinated 9-methylfluorene (5
