反应详情

To a solution of 5-Methoxy-1-methyl-1H-indole-3-carbaldehyde (4.5 g, 23.8 mmol, in 150 ml DCM) was added BBr3 solution (2 M in DCM, 60 ml, 5 eq) at −10° C. with stirring for 5 min. The cooling bath was removed and the reaction mixture was slowly warmed up to r.t. The reaction was monitored by TLC (2% MeOH in DCM) and LCMS (after 3.5 h, no starting material remained). The reaction mixture was then cooled to −10° C., and 16 ml of MeOH were slowly added. The pH of mixture was adjusted to 8 by adding sat. NaHCO3 and/or 4 N NaOH. The organic solvents were removed under reduced pressure and the remaining aqueous mixture was extracted with ethyl acetate (30 ml×5). The organic layers were combined, washed with brine (10 ml×1), dried over Mg2SO4, filtered and dried under reduced pressure to give the title compound as 4.06 g purple powder (yield: 97%) that was used without further purification. LCMS (2-85% ACN/H2O in 7 min): 176.1 (40%). Rf 0.11 (2% MeOH in DCM).

1. customThe cooling bath was removed
2. customafter 3.5 h
3. temperatureThe reaction mixture was then cooled to −10° C.
4. addition16 ml of MeOH were slowly added
5. additionby adding sat. NaHCO3 and/or 4 N NaOH
6. customThe organic solvents were removed under reduced pressure
7. extractionthe remaining aqueous mixture was extracted with ethyl acetate (30 ml×5)
8. washwashed with brine (10 ml×1)
9. dry with materialdried over Mg2SO4
10. filtrationfiltered
11. customdried under reduced pressure