HRID554190

反应详情

EQUATION

反应方程式

HRID 554190 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A solution of (10 mL) ethyl 4-methyl-1-[(4-methylphenyl)sulfonyl]-5-phenyl-1H-pyrrole-3-carboxylate (420 mg) in tetrahydrofuran was cooled to −78° C., a 1.5 mol/l solution (2.1 mL) of diisobutylaluminum hydride in toluene was added dropwise, and the mixture was further stirred at −78° C. for 30 min. 1 mol/l Hydrochloric acid (10 mL) was added to the reaction mixture, and the mixture was stirred at room temperature and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. A solution (15 mL) of the residue in acetonitrile was cooled to −78° C., tetra-n-propylammonium perruthenate (37 mg), N-methylmorpholine N-oxide (185 mg) and molecular sieves 4A powder (1.0 g) were added, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, and the residue was suspended in ethyl acetate and filtered through celite. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→1:1) to give the title compound as a brown oil (yield 320 mg, 90%).

WORKUP

后处理

  1. stirringthe mixture was stirred at room temperature
  2. extractionextracted with ethyl acetate
  3. washThe extract was washed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. temperatureA solution (15 mL) of the residue in acetonitrile was cooled to −78° C.
  7. additiontetra-n-propylammonium perruthenate (37 mg), N-methylmorpholine N-oxide (185 mg) and molecular sieves 4A powder (1.0 g) were added
  8. stirringthe mixture was stirred at room temperature for 1 hr
  9. concentrationThe reaction mixture was concentrated under reduced pressure
  10. filtrationfiltered through celite
  11. concentrationThe filtrate was concentrated under reduced pressure
  12. customthe residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=9:1→1:1)