Nitriles can be reduced to primaryamines by reduction, using the reducing agent lithiumaluminiumhydride. This is a much more efficient method of producing primaryaliphaticamines than halogenoalkanes.
The reagents in the preparation of primaryaliphaticamine from nitriles are mixed in dry ether. This removes any water (impurity) that could affect the reaction outcome.
One disadvantage of the preparation of primaryaliphaticamines from nitriles is that it is a two step reaction, meaning it could result in a lower yield of primaryamine.