The nucleophilic 1,2-addition of formaldehyde N,N-dialkylhydrazones 1, 2, and 7-10 to trifluoromethyl ketones 3a-e takes place in the absence of any catalyst or promoter to afford a series of alpha-hydroxy-alpha-trifluoromethylhydrazones (4, 5, and 11-14) in good-to-excellent yields. From the several reagents studied, optimal results were achieved using 1-(methyleneamino)pyrrolidine (2) for the synthesis of racemic adducts and (S)-1-(methyleneamino)-2-[1-(methoxy)diphenyl-methyl]-pyrrolidine (10) for the asymmetric version of the reaction. The resolving properties of the chiral auxiliary carried by 10 allowed an easy chromatographic (flash) separation of any obtained diastereomeric mixture. Thus, a single operation rendered moderate-to-good amounts (42-75%) of optically pure adducts (S,S)-14 (de >/= 98%) by combining excellent chemical (82-92%) and moderate optical (51-81%) yields. Hydrazones 5 and (S,S)-14 were protected by benzylation [--> 16 and (S,S)-18] and then transformed into benzyl-protected alpha-trifluoromethyl cyanohydrins 21 by MMPP oxidative cleavage and into alpha-benzyloxy-alpha-trifluoromethyl aldehydes 22 by ozonolysis. Alternatively, adducts 5 and (S,S)-14 were methylated [--> 19 and (S,S)-20] and transformed into the corresponding alpha-methoxy-alpha-trifluoromethyl carboxylic acids 24 by successive ozonolysis and in situ oxidation (NaClO(2), (t)()BuOH, isobutene) of the crude alpha-methoxyaldehydes.