The reagent on the left, reactive with HCl, H20 and heat, to make the product on the right. It also made to other products including the one on the right. They are not HCl or H20. Can someone provide a mechanism for this reaction?
This is double hydrolysis, one is the amide(CONH) and the other one is an ester hydrolysis(COO), so you'd get the carboyxlic acid derivative, then you'd also get (NH2)CH2(COOH) and you also get CH3OH.
hey