1,1,1-Triaryl-2,2,2-trifluoroethanes and process for their synth

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

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260386, 570123, 570129, 528402, C07C 1700, C07C 1724, C07C 1726, C07C 1908

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active

043070248

ABSTRACT:
New 1,1,1-triaryl-2,2,2-trifluoroethanes in which the aryl radicals carry one or more substitutents have been prepared by condensation of trifluoroacetophenones with substituted phenyl compounds in the presence of catalytic quantities of trifluoromethylsulfonic acid. The reaction can be carried out under reflux in toluene or, for strikingly better results in certain cases, reactants are simply stirred at room temperature for about 24 to 48 hours.

REFERENCES:
Hey et al., Chemical Abstracts, vol. 54, Cols. 8710 to 8714 (1960).
Steadman, Chemical Abstracts, vol. 79, Item 104937h (1973).
Kray et al., J. Organic Chemistry, vol. 42, No. 7, pp. 1186 to 1189 (1977).

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