Imine

Imines are typically prepared by the condensation of primary amines and aldehydes or ketones.[12][13] Ketones undergo similar reactions, but less commonly than aldehydes. In terms of mechanism, such reactions proceed via the nucleophilic addition giving a hemiaminal -C(OH)(NHR)- intermediate, followed by an elimination of water to yield the imine (see alkylimino-de-oxo-bisubstitution for a detailed mechanism). The equilibrium in this reaction usually favors the carbonyl compound and amine, so that azeotropic distillation or use of a dehydrating agent, such as molecular sieves or magnesium sulfate, is required to favor of imine formation. In recent years, several reagents such as Tris(2,2,2-trifluoroethyl)borate [B(OCH₂CF₃)₃],[14] pyrrolidine[15] or titanium ethoxide [Ti(OEt)₄][16] have been shown to catalyse imine formation.

Rarer than primary amines is the use of ammonia to give a primary imine.[17] In the case of hexafluoroacetone, the hemiaminal intermediate can be isolated.[18]

Primary ketimines can be synthesized via a Grignard reaction with a nitrile. This method is known as Moureu-Mignonac ketimine synthesis.[19] [20][21] For example, benzophenone imine can also be synthesized by addition of phenylmagnesium bromide to benzonitrile followed by careful hydrolysis (lest the imine be hydrolyzed):[22]

C₆H₅CN + C₆H₅MgBr → (C₆H₅)₂C=NMgBr

(C₆H₅)₂C=NMgBr + H₂O → (C₆H₅)₂C=NH + MgBr(OH)

Several other methods exist for the synthesis of imines.

• Reaction of organic azides with metal carbenoids (produced from diazocarbonyl compounds).[23]
• Condensation of carbon acids with nitroso compounds.
• The rearrangement of trityl N-haloamines in the Stieglitz rearrangement.
• By reaction of alkenes with hydrazoic acid in the Schmidt reaction.
• By reaction of a nitrile, hydrochloric acid, and an arene in the Hoesch reaction.
• Multicomponent synthesis of 3-thiazolines in the Asinger reaction.
• Thermal decomposition of oximes.[24]

The chief reaction of imines, often undesirable, is their hydrolysis back to the amine and the carbonyl precursor.

R₂C=NR' + H₂O ⇌ R₂C=O + R'NH₂

Imines are widely used as intermediates in the synthesis of heterocycles.

• Aromatic imines react with an enol ether to a quinoline in the Povarov reaction.
• Imines react, thermally, with ketenes in [2+2] cycloadditions to form β-lactams in the Staudinger synthesis.[25] Several variants have been described.[26][27]
• Imine react with dienes in the Imine Diels-Alder reaction to a tetrahydropyridine.
• tosylimines react with α,β-unsaturated carbonyl compound to give allylic amines in the Aza-Baylis–Hillman reaction.

Somewhat like the parent amines, imines are mildly basic and reversibly protonate to give iminium salts:

R₂C=NR' + H⁺ ${\displaystyle {\ce {<=>>}}}$ [R₂C=NHR']⁺

Alternatively, primary imines are sufficiently acidic to allow N-alkylation, as illustrated with benzophenone imine:[28]

(C₆H₅)₂C=NH + CH₃Li → (C₆H₅)₂C=NLi + CH₄

(C₆H₅)₂C=NLi + CH₃I → (C₆H₅)₂C=NCH₃ + LiI

Imines are common ligands in coordination chemistry. Particularly popular examples are found with Schiff base ligands derived from salicylaldehyde, the salen ligands. Metal-catalyzed reactions of imines proceed through such complexes. In classical coordination complexes, imines bind metals through nitrogen. For low-valent metals, η²-imine ligands are observed.

Very analogous to ketones and aldehydes, primary imines are susceptible to attack by carbanion equivalents. The method allow for the synthesis of secondary amines:[29][30]

R₂C=NR' + R"Li → R₂R"CN(Li)R'

R₂R"CN(Li)R' + H₂O → R₂R"CNHR' + LiOH

Imines are reduced via reductive amination. An imine can be reduced to an amine via hydrogenation for example in a synthesis of m-tolylbenzylamine:[31]

Other reducing agents are lithium aluminium hydride and sodium borohydride.[32]

The asymmetric reduction of imines has been achieved by hydrosilylation using a rhodium-DIOP catalyst.[33] Many systems have since been investigated.[34][35]

Owing to their enhanced electrophilicity, iminium derivatives are particularly susceptible to reduction to the amines. Such reductions can be achieved by transfer hydrogenation or by the stoichiometric action of sodium cyanoborohydride. Since imines derived from unsymmetrical ketones are prochiral, their reduction defines a route to chiral amines.

Unhindered aldimines tend to cyclize, as illustrated by the condensation of methylamine and formaldehyde, which gives the hexahydro-1,3,5-triazine.

Imine polymers (polyimines) can be synthesised from multivalent aldehydes and amines.[36] The polymerisation reaction proceeds directly when the aldehyde and amine monomers are mixed together at room temperature. In most cases, (small) amounts of solvent may still be required. Polyimines are particularly interesting materials because of their application as vitrimers. Owing to the dynamic covalent nature of the imine bonds, polyimines can be recycled relatively easily. Furthermore, polyimines are known for their self-healing behaviour.[37][38]

Akin to pinacol couplings, imines are susceptible to reductive coupling leading to 1,2-diamines. [39]

Imine are oxidized with meta-chloroperoxybenzoic acid (mCPBA) to give an oxaziridines.

Imines are intermediates in the alkylation of amines with formic acid in the Eschweiler-Clarke reaction.

A rearrangement in carbohydrate chemistry involving an imine is the Amadori rearrangement.

A methylene transfer reaction of an imine by an unstabilised sulphonium ylide can give an aziridine system. Imine react with dialkylphosphite in the Pudovik reaction and Kabachnik–Fields reaction