I saw a post about the basic hydrolysis of n methyl acetamide, but am wondering if anyone can speculate if acidic hydrolysis by formic acid would also work?
My thinking being, if it works, the n methylacetamide will hydrolyze into methylamine, and acetic acid, and since formic acid is the stronger acid, it should form methylammonium formate, and acetic acid.
Does this sound right?
My thinking being, if it works, the n methylacetamide will hydrolyze into methylamine, and acetic acid, and since formic acid is the stronger acid, it should form methylammonium formate, and acetic acid.
Does this sound right?