react anniline with NaNO2 and HCl in 273-278K to get benzene diazonium chloride.React this with CuCN and KCN to get a benzonitrile.Reduce this in presence of LiAlH4 or Ni/Pd catalyst to get benzylamine. hope u get it!
The f irst project describes the synthesis of 4-arylhexahy&opy~olo[3,2-c]quinolines. The one pot ... electron donating groups on the aniline results in impure products. ...... hexahydropyrrolo[3,2-clquinoline-1-carbothioic acid benzylamide. (56)
Raghuvaran varan Chandragiri
Last Activity: 12 Years ago
Aniline is more basic due to the strong electron withdrawing effect of the carbonyl oxygen on the amide of acetanilide.
Aniline is more basic due to the strong electron withdrawing effect of the carbonyl oxygen
Aniline is much less basic than cyclohexyl amine
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