反应详情

Add hexyl magnesium bromide (2.0M in ethyl ether, 8 mL, 16 mmol) to 4′-trifluoromethyl-biphenyl-4-carbaldehyde (2.0 g, 8 mmol) (prepared in a manner substantially similar to preparation 25, or other methods known in the art) in tetrahydro-furan (30 mL) at 0° C. under inert atmosphere. Stir 1.5 hours. Quench reaction with saturated solution of ammonium chloride, dilute with ethyl acetate. Wash organic phase with water then saturated sodium chloride solution. Dry organic fraction with Na2SO4, filter, and concentrate under reduced pressure. Purify on silica gel chromatography (0-30% Ethyl acetate/hexanes gradient) to provide 1.95 g of title compound (73%).

1. customprepared in a manner substantially similar to preparation 25, or other methods
2. customat 0° C.
3. customQuench
4. customreaction with saturated solution of ammonium chloride
5. filtrationDry organic fraction with Na2SO4, filter
6. concentrationconcentrate under reduced pressure
7. customPurify on silica gel chromatography (0-30% Ethyl acetate/hexanes gradient)