J. Yamamoto et al., FRIEDEL-CRAFAFTS DIPHENYLMETHYLATION OF B ENZENE WITH DIPHENYLMETHANOLS USING IRON(III) CHLORIDE, Nippon kagaku kaishi, (8), 1993, pp. 988-990
When a mixture of diphenylmethamols and iron(III) chloride (FeCl3) was
heated in benzene, Friedel-Crafts' diphenylmethylation took place to
yield triphenylmethanes with the corresponding benzophenones as by-pro
ducts. [GRAPHICS] X; H, o-CH3, m-CH3, p-CH3 P-Cl, p-NO2 The yield of t
riphenylmethanes could be elevated without a formation of benzophenone
s by adding a small amount of tribenzylamine to the benzene solution o
f diphenylmethanols and FeCl3. [GRAPHICS] X; H, o-CH3, m-CH3, p-CH3, p
-Cl, p-NO2 Pentylamine and hydroquinone could be used to get more yiel
d of triphenylmethane in the reaction of benzene with diphenylmethanol
.