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Primary aromatic amines crystalline derivatives

Primary aliphatic amines, 413 crystalline derivatives of, 424 reactions of, 420, 1072 table of, and derivatives of, 424 Primary aromatic amines, 539 crystalline derivatives of, 652 reactions and characterisation of, 648, 1073 ... [Pg.1183]

Secondary amines can be prepared from the primary amine and carbonyl compounds by way of the reduction of the derived Schiff bases, with or without the isolation of these intermediates. This procedure represents one aspect of the general method of reductive alkylation discussed in Section 5.16.3, p. 776. With aromatic primary amines and aromatic aldehydes the Schiff bases are usually readily isolable in the crystalline state and can then be subsequently subjected to a suitable reduction procedure, often by hydrogenation over a Raney nickel catalyst at moderate temperatures and pressures. A convenient procedure, which is illustrated in Expt 6.58, uses sodium borohydride in methanol, a reagent which owing to its selective reducing properties (Section 5.4.1, p. 519) does not affect other reducible functional groups (particularly the nitro group) which may be present in the Schiff base contrast the use of sodium borohydride in the presence of palladium-on-carbon, p. 894. [Pg.902]


See other pages where Primary aromatic amines crystalline derivatives is mentioned: [Pg.28]    [Pg.108]    [Pg.301]    [Pg.272]   
See also in sourсe #XX -- [ Pg.652 ]

See also in sourсe #XX -- [ Pg.652 ]

See also in sourсe #XX -- [ Pg.652 ]




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Amination primary

Amines derivatives

Amines primary

Aromatic amination

Aromatic amines

Aromatic amines Derivatives

Aromatics amination

Crystalline derivatives

Primary aromatic

Primary aromatic amines

Primary derivatives

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