反应详情

To a solution of 7-chloroindole (4.91 g, 32.4 mmol) in dimethylformamide (60 ml) at 0° C. under nitrogen was added sodium hydride (60% dispersion in mineral oil, 1.43 g, 35.6 mmol). The mixture was stirred for 1 h at room temperature. Cyclohexylmethyl bromide (5.0 ml, 35.6 mmol) was added at 0° C. The mixture was stirred for 18 h at room temperature. To the reaction mixture was added sodium hydride (60% dispersion in mineral oil, 358 mg, 8.94 mmol). After stirring for 15 mins, cyclohexylmethyl bromide (1.25 ml, 8.96 mmol) was added. The mixture was heated at 70° C. with stirring for 1.5 h. After cooling to room temperature, the mixture was partitioned between dichloromethane and water. The aqueous layer was extracted with dichloromethane and combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The obtained residue was purified by column chromatography eluting with 0-5% (v/v) ethyl acetate in n-heptane to afford 7-chloro-1-cyclohexylmethylindole (8.1 g, 32.0 mmol).

1. stirringThe mixture was stirred for 18 h at room temperature
2. stirringAfter stirring for 15 mins
3. temperatureThe mixture was heated at 70° C.
4. stirringwith stirring for 1.5 h
5. temperatureAfter cooling to room temperature
6. customthe mixture was partitioned between dichloromethane and water
7. extractionThe aqueous layer was extracted with dichloromethane
8. washwere washed with brine
9. dry with materialdried over sodium sulfate
10. concentrationconcentrated in vacuo
11. customThe obtained residue was purified by column chromatography
12. washeluting with 0-5% (v/v) ethyl acetate in n-heptane