Producing Amines (Cambridge (CIE) A Level Chemistry): Revision Note

Exam code: 9701

Caroline Carroll

Written by: Caroline Carroll

Reviewed by: Lucy Kirkham

Updated on

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

Structures of primary and secondary amines

Structures of a primary amine, ethylamine CH3CH2NH2 (R-NH2, one alkyl group on nitrogen), and a secondary amine, N-methylphenylamine (R1NH-R2, one alkyl and one aryl group on nitrogen)

A primary amine has one R-group attached to the nitrogen atom, while a secondary amine has two R-groups attached to the nitrogen atom

  • 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

Chloroethane heated with two moles of ammonia in ethanol gives ethylamine (a primary amine) and ammonium chloride

Primary amines can be produced by a nucleophilic substitution of a halogenoalkane with an excess of ammonia

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

Chloroethane heated with ethylamine in ethanol gives diethylamine (a secondary amine) and hydrogen chloride

Secondary amines can be produced by a nucleophilic substitution of a halogenoalkane with a primary 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

Formation of amines from amides

Reduction of amides with LiAlH4: ethanamide with 4[H] gives ethylamine (primary amine) and water; N-methylethanamide with 4[H] gives N-methylethylamine (secondary amine) and water

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 to form a primary amine

Formation of amines from nitriles

Reduction of ethanenitrile to ethylamine, either with 4[H] from LiAlH4 or with 2H2 over a nickel catalyst

Nitriles can be reduced with LiAlH4 or H2 and Ni catalyst

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Caroline Carroll

Author: Caroline Carroll

Expertise: Head of Content Delivery

Caroline graduated from the University of Nottingham with a degree in Chemistry and Molecular Physics. She spent several years working as an Industrial Chemist in the automotive industry before retraining to teach. Caroline has over 12 years of experience teaching GCSE and A-level chemistry and physics. She is passionate about delivering high-quality resources to help students achieve their full potential.

Lucy Kirkham

Reviewer: Lucy Kirkham

Expertise: Content Creator

Lucy has been a passionate Maths teacher for over 12 years, teaching maths across the UK and abroad helping to engage, interest and develop confidence in the subject at all levels.Working as a Head of Department and then Director of Maths, Lucy has advised schools and academy trusts in both Scotland and the East Midlands, where her role was to support and coach teachers to improve Maths teaching for all.