Carbonyl Addition Condensations of Diphenylmethane Involving Methylene Hydrogen by Alkali Amides. Synthesis of Certain Benzhydryl Type Carbinols1, 2
PJ Hamrick Jr, CR Hauser
Index: Hamrick; Hauser Journal of the American Chemical Society, 1959 , vol. 81, p. 2096,2099
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Citation Number: 5
Abstract
As can be seen from Scheme A, the equilibrium of the addition reaction is considered to be far on the side of the alkali salt of the carbinol Ia. Evidence for this is the observation that the characteristic red color of the diphenylmethide ion is discharged by a molecular equivalent of the ketone. Moreover, this explains the high yields of the carbinol I obtained when the reaction mixture is poured into excess ammonium chloride, under which conditions the ...
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