Trifluoroacetic Acid Hydroxylamine System as Organocatalyst Reagent in a One-Pot Salt Free Process for the Synthesis of Caprolactam and Amides of Industrial Interest
Abstract
In this work we studied the reactivity of the Trifuoroacetic acid hydroxylamine system in the one step salt free synthesis of
amides from ketones. A particular regards was paid to the caprolactam synthesis because of its industrial relevance. Synthesis, reactivity and characterization of the hydroxylamine trifuoroacetate is given. Fast oximation reaction of several ketones
was gained at room temperature (1 h of reaction quantitative conversion for several ketones). In the same reactor, by raising
the temperature at 383 K, the Beckmann rearrangement of the so obtained oximes is easily accomplished in the presence of
three equivalent of TFA. The possibility of obtaining the trifuoroacetate of the hydroxylamine with a modifed nitric acid
hydrogenation reactions was verifed, too. Reuse of solvent and trifuoroacetic acid is easily achieved by distillation.
