Production of Primary & Secondary Amines
- Primary amines are organic compounds that have an -NH2 functional group attached to an alkyl or aryl group
- Secondary amines have two alkyl or aryl groups attached to an -NH group
Primary and secondary amines
- Primary and secondary amines can be prepared from different reactions including:
- The reaction of halogenoalkanes with ammonia
- The reaction of halogenoalkanes with primary amines
- The reduction of amides
- The reduction of nitriles
Reaction of halogenoalkanes with ammonia
- This is a nucleophilic substitution reaction in which the nitrogen lone pair in ammonia acts as a nucleophile and replaces the halogen in the halogenoalkane
- When a halogenoalkane is reacted with excess, hot ethanolic ammonia under pressure a primary amine is formed
Formation of primary amine
Reaction of halogenoalkanes with primary amine
- This is also a nucleophilic substitution reaction in which the nitrogen in the primary amine acts as a nucleophile and replaces the halogen in the halogenoalkane
- When a halogenoalkane is reacted with a primary amine in ethanol and heated in a sealed tube, under pressure a secondary amine is formed
Formation of secondary amine
Reduction of amides
- Amines can also be formed from the reduction of amides by LiAlH4 in dry ether
- Whether a primary or secondary amine is formed depends on the nature of the amide
Amides can be reduced by LiAlH4 to form amines
Reduction of nitriles
- Nitriles contain a -CN functional group which can be reduced to an -NH2 group
- The nitrile vapour and hydrogen gas are passed over a nickel catalyst or LiAlH4 in dry ether can be used to form a primary amine
Nitriles can be reduced with LiAlH4 or H2 and Ni catalyst