A primary amine, RNH2 can be reacted with CH3−X to get secondary amine, R−NHCH3 but the only disadvantage is that 3∘ amine and quaternary ammonium salts are also obtained as side products. Can you suggest a method where RNH2 forms only 2∘ amine?
Carbylamine reaction can be used to produce a secondary amine only from primary amine. This reaction is shown by 1∘ amine only which results in the replacement of two hydrogen atoms attached to the nitrogen atom of NH2 group by one carbon atom. On catalytic reduction, the isocyanide will give a secondary amine with one methyl group.
RNH2KOH+CHCl3−−−−−−−−−→RNCH2/Pd−−−−→RNHCH3