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Rhodium trifluoromethyl derivatives

The compounds benzonitrile, p-methylbenzonitrile, /)-methoxybenzonitrile, p-trifluoromethyl-benzonitrile, /)-methoxycarbonylbenzonitrile, and triethoxysilane are commercial products and are degassed and stored under argon before use. Trimethylsilane was prepared according to a literature report [38]. The nitrile (9.8 mmol) and the hydrosilane (49 mmol) are added to the rhodium catalyst (0.1 mmol) contained in a Carius tube. When using trimethylsilane, the operation is performed at —20°C. The tube is closed and the mixture stirred at 100 °C for 15h. The liquid is separated by filtration and the excess of hydrosilane removed under vacuum to leave the N, Wdisilylamine derivative. If necessary, a bulb to bulb distillation is performed to obtain a completely colorless liquid. The yields obtained in the different runs are reported in Table 6. The product have been characterized by elemental analysis, NMR spectroscopy, and GC-MS analysis. [Pg.450]

Scheme 39.2 Examples of typical rhodium-based catalyst systems and modified derivatives of triphenylphosphine as used to control their solubility with scC02 in homogeneous or multiphase systems (BARF=tetrakis[3,5-bis (trifluoromethyl)phenyl]borate). Scheme 39.2 Examples of typical rhodium-based catalyst systems and modified derivatives of triphenylphosphine as used to control their solubility with scC02 in homogeneous or multiphase systems (BARF=tetrakis[3,5-bis (trifluoromethyl)phenyl]borate).

See other pages where Rhodium trifluoromethyl derivatives is mentioned: [Pg.205]    [Pg.165]    [Pg.169]    [Pg.1365]    [Pg.245]    [Pg.206]    [Pg.339]    [Pg.334]    [Pg.122]   
See also in sourсe #XX -- [ Pg.303 , Pg.304 , Pg.305 ]




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Rhodium derivatives

Trifluoromethyl derivatives

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