Why cannot aromatic primary amines be prepared by Gabriel phthalimide synthesis?

Answer 1

aromatic primary amine canot be synthesised by gabriel phthamide synthesys as aryl halide does not show nucliophilic substitution reaction

Answer 2

Aromatic primary amines cannot be prepared by the Gabriel phthalimide synthesis because the nitrogen atom in the aromatic primary amine is not sufficiently nucleophilic to displace the phthalimide leaving group. The reaction typically requires a primary alkyl halide, which is more reactive toward nucleophilic substitution than an aromatic primary amine.