반응 #654558
ord-36b4eb5564264aae8defa89d43121e36
반응 방정식
용매
반응 조건
후처리
- 1기타The layers were separated
- 2추출the aqueous phase was extracted with EtOAc (2×200 mL)
- 3세척The combined organic layers were washed with H2O (4×500 mL)
- 4건조dried over Na2SO4
- 5여과filtered
- 6농축concentrated in vacuo
- 7기타The crude residue was purified by flash chromatography (SiO2; hexanes)
실험 절차
NaH (7.7 g, 191.7 mmol) was added portionwise to a 0° C. solution of 4-methoxyindole (21.7 g, 147 mmol) in 750 mL of anhydrous DMF. After 15 min, the slurry was treated with benzyl bromide (17.5 mL, 147 mmol). The reaction mixture was allowed to warm to ambient temperature and stir overnight. The reaction mixture was poured into 1 L of H2O. The layers were separated, and the aqueous phase was extracted with EtOAc (2×200 mL). The combined organic layers were washed with H2O (4×500 mL), dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (SiO2; hexanes) to give 32.9 g (138.6 mmol; 94%) of the title compound as a white solid. Electrospray MS 238 (M+1);