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Lithium bromide monoxide

Lithium monobromide. See Lithium bromide Lithium monohydride. See Lithium hydride Lithium monoxide. See Lithium oxide Lithium nitrate... [Pg.2424]

In the carbonylation reactions, further reaction of the acyl lithium compounds with carbon monoxide can occur, but clean reaction can be achieved if the lithium amide is first converted to a copper derivative (Scheme 130) (79JOC3734). In the case of morpholine, reaction with allyl bromide gave a 93% overall yield of the amide product. [Pg.259]

S-BROMOAMINES Diethyl dibromophosphoramidate. a-BROMOCARBONYE COMPOUNDS Bromine. Magneaum bromide. a -BUTENOLIDES Carbon monoxide. Sodium methylsulfinylmethylide. f-BUTYL KETONES Lithium phenylthio(r-butyl)cupiate(I). [Pg.469]

Heating A, Af -diphenylurea with amines (butylamine, cyclohexylamine, benzylamine, 2,6-diethylaniline or morpholine) in DMF in the presence of triethylamine yields unsym-metrical ureas, e.g. PhNHCONHBu from butylamine . High yields of isocyanates RNCO are obtained in the reactions of primary aliphatic amines, carbon dioxide and triethylamine with phosphorus oxychloride . Treatment of secondary amines with butylUthium, followed by carbon monoxide at —78 °C under atmospheric pressure, sulphur and an alkyl halide affords 5-alkyl thiocarbamates, e.g. Et2NC(0)SCH2Ph from diethylamine and benzyl bromide. The key step in the sequence is the generation of the lithium thiocarbamate shown in equation 112 . [Pg.596]


See other pages where Lithium bromide monoxide is mentioned: [Pg.1375]    [Pg.1425]    [Pg.251]    [Pg.35]    [Pg.596]    [Pg.86]    [Pg.97]    [Pg.154]    [Pg.515]    [Pg.533]    [Pg.785]    [Pg.790]    [Pg.826]    [Pg.940]    [Pg.981]    [Pg.984]    [Pg.1051]    [Pg.12]    [Pg.705]    [Pg.951]    [Pg.24]    [Pg.246]    [Pg.1126]    [Pg.266]    [Pg.185]   
See also in sourсe #XX -- [ Pg.486 ]

See also in sourсe #XX -- [ Pg.486 ]




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Lithium bromide

Lithium monoxide

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