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Lithium aluminum hydride acyl halides

The use of acyl azides in the preparation of amines by the Curtius rearrangement has been discussed previously (Section 23-12E). Alkyl azides can be reduced readily by lithium aluminum hydride to amines and, if a pure primary amine is desired, the sequence halide — azide — amine may give as good or better results than does the Gabriel synthesis (Section 23-9D). [Pg.1202]


See other pages where Lithium aluminum hydride acyl halides is mentioned: [Pg.887]    [Pg.95]    [Pg.539]    [Pg.97]    [Pg.237]    [Pg.236]    [Pg.887]    [Pg.260]    [Pg.263]    [Pg.445]    [Pg.887]    [Pg.445]    [Pg.145]    [Pg.353]    [Pg.464]    [Pg.887]    [Pg.847]    [Pg.552]    [Pg.1773]    [Pg.445]   
See also in sourсe #XX -- [ Pg.241 , Pg.263 ]

See also in sourсe #XX -- [ Pg.8 , Pg.241 , Pg.263 ]

See also in sourсe #XX -- [ Pg.8 , Pg.241 , Pg.263 ]




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Acyl aluminum

Acyl-lithium

Aluminum halides

Halides lithium

Hydride halides

Lithium acylation

Lithium hydride acyl halides

Lithiums aluminum halides

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