反应详情

n-BuLi (2.5N, 8.0 mL) was added at −78° C. to a mixture of methyltriphenylphosphonium bromide (5.6 g, 0.15 mol) in THF (50 mL). After being stirred for 0.5 hours, 2-(tert-butyldimethylsilyloxy)-1-(4-chloro-3-fluorophenyl)ethanone (3.9 g, 0.013 mol) was added to the reaction mixture. The mixture was then stirred for 2 hours at 25° C. After quenching with saturated NH4CL (100 mL), the reaction mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried and concentrated. The residue was purified by silica gel column chromatography eluting with petroleum ether to give tert-butyl (2-(4-chloro-3-fluorophenyl)allyloxy)dimethylsilane (1.6 g, 40% yield).

1. stirringThe mixture was then stirred for 2 hours at 25° C
2. customAfter quenching with saturated NH4CL (100 mL)
3. extractionthe reaction mixture was extracted with ethyl acetate (3×50 mL)
4. customThe combined organic layers were dried
5. concentrationconcentrated
6. customThe residue was purified by silica gel column chromatography
7. washeluting with petroleum ether