We studied the reaction of propiophenone with diethylamine and paraformalde
hyde to produce beta-dimethylamino-alpha-methyl-propiophenone hydrochloride
in P-propanol. Mle have found two steps, the first: the reaction of diethy
lamine with paraformaldehyde, which gives equilibrium without water elimina
tion. The second, after ketone is added, is slower sand irreversible. The w
hole Mannich reaction can be represented by a third order reaction, which i
ndicates that the intermediary is a cation imonium.