HRID1725377

反应详情

EQUATION

反应方程式

HRID 1725377 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Add tert-butyl lithium (27.07 ml, 46.03 mmol, 1.7 M in pentane) to a solution of 4-Bromo-1-[3-(tert-butyldimethyl-silyloxy)prop-1-yl]-1H-indole (6.76 g, 18.41 mmol) in anhydrous tetrahydrofuran (100 ml) at −78° C. Stir the reaction at −78° C. for 30 min, quench with N,N-dimethylformamide (4.7 ml, 64.45 mmol), warm to O° C., quench with pH=7 buffer, and extract into ethyl acetate. Combine the organic layers, dry over magnesium sulfate, and concentrate under reduced pressure. Purification by flash chromatography, eluting with ethyl acetate: hexane gradient (100% hexane to 50% ethyl acetate: hexane over 45 minutes) gives the title compound as a clear oil.

WORKUP

后处理

  1. customthe reaction at −78° C. for 30 min
  2. temperaturewarm to O° C
  3. custom, quench with pH=7 buffer
  4. extractionextract into ethyl acetate
  5. dry with materialdry over magnesium sulfate
  6. concentrationconcentrate under reduced pressure
  7. customPurification by flash chromatography
  8. washeluting with ethyl acetate