HRID2194929

反应详情

EQUATION

反应方程式

HRID 2194929 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

5-bromo-1-(methylsulphonyl)indoline (13.4 mmol, 3.7 g) and ethyl-2-chloropropionate (17.4 mmol, 2.38 g) were dissolved in DMF (7 ml) in a protective gas atmosphere at room temperature. Subsequently, manganese (26.8 mmol, 1.47 g), (2,2′-bipyridine) nickel(II)-dibromide (0.938 mmol, 0.351 g) and TFA (0.348 mmol, 27 μl) were added and stirring was carried out at 50° C. for 1.5 h. After cooling the reaction mixture to room temperature, hydrolysis was carried out at room temperature with 1 N HCl (25 ml) and the mixture was extracted with diethyl ether (3×25 ml). The combined organic phases were washed with water (25 ml) and aq. sat. NaCl solution (25 ml) and dried over magnesium sulphate. After removing the solvent in a vacuum and purifying the residue by column chromatography (SiO2, diethyl ether/hexane=3:1), 0.558 g (14% yield) of ethyl 2-(1-(methylsulphonyl)indolin-5-yl)propanoate were obtained.

WORKUP

后处理

  1. customhydrolysis
  2. extractionthe mixture was extracted with diethyl ether (3×25 ml)
  3. washThe combined organic phases were washed with water (25 ml) and aq. sat. NaCl solution (25 ml)
  4. dry with materialdried over magnesium sulphate
  5. customAfter removing the solvent in a vacuum
  6. custompurifying the residue by column chromatography (SiO2, diethyl ether/hexane=3:1)