Diethyl Ether → 5-(Benzyloxy)-3-methyl-1H-indole

To a solution of 5-benzyloxyindole (19.8 g, 88.68 mmol) in THF (200 mL) pre-cooled with an ice bath, was added a 3.0 M solution of ethyl magnesium bromide in diethyl ether (44.3 mL, 133.02 mmol). The ice bath was removed and the resulting mixture was gradually warmed to rt over 5 h. The reaction mixture was cooled to 0° C. and iodomethane (37.8 g, 266.04 mmol) was added. The mixture was warmed to rt and stirred for 12 h. The reaction mixture was quenched by the addition of saturated aqueous ammonium chloride solution (50 mL). The reaction mixture was diluted with diethyl ether (150 mL), and then washed with water and a brine solution consecutively. The combined organic layers were dried over magnesium sulfate, filtered, and then concentrated via rotary evaporation to give a dark brownish solid. The crude mixture was purified on silica gel (95:5 hexane: dichloromethane) to give the title compound (12.6 g, 60%) as a brown solid. 1H NMR (400 MHz, CDCl3) δ 7.79 (br s, 1H), 7.50 (d, 2H), 7.45 (m, 3H), 7.32 (s, 1H), 7.11 (d, 1H), 6.95 (m, 2H), 5.13 (s, 2H), 2.31 (s, 3H).

1. customThe ice bath was removed
2. temperatureThe reaction mixture was cooled to 0° C.
3. temperatureThe mixture was warmed to rt
4. customThe reaction mixture was quenched by the addition of saturated aqueous ammonium chloride solution (50 mL)
5. additionThe reaction mixture was diluted with diethyl ether (150 mL)
6. washwashed with water
7. dry with materialThe combined organic layers were dried over magnesium sulfate
8. filtrationfiltered
9. concentrationconcentrated via rotary evaporation
10. customto give a dark brownish solid
11. customThe crude mixture was purified on silica gel (95:5 hexane: dichloromethane)

ORD record

ord-9b09866b22b94eddabba835d6610129c

Source dataset

uspto-grants-2011_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07964622B2