HRID1821936

反应详情

EQUATION

反应方程式

HRID 1821936 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

0.325 g (1.50 mmol) tert-butylindole-2-carboxylate is dissolved in 15 ml absolute DMSO, mixed with 0.184 g (1.64 mmol) potassium-tert-butylate and stirred at 110° C. for 15 min. A solution of 0.576 g (1.50 mmol) [1-bromo-3-(4-octylphenoxy)propan-2-yl]acetate in 15 ml absolute DMSO is added drop-wise. Following 30 minutes of heating at 110° C. and subsequent cooling, hydrolysis is carried out in saturated NaCl solution. Four extractions with diethyl ether, combination of the organic phases, concentration to half the volume on the rotary evaporator, three wash steps with saturated NaCl solution, drying on sodium sulfate, filtration and reconcentration on the rotary evaporator leave as a crude product a yellow oil which is purified on silica gel by means of flash column chromatography (flow agent: petroleum ether/ethyl acetate 99:1) and yields the product as a colorless oil.

WORKUP

后处理

  1. waitFollowing 30 minutes
  2. temperatureof heating at 110° C.
  3. customsubsequent cooling, hydrolysis
  4. extractionFour extractions
  5. concentrationwith diethyl ether, combination of the organic phases, concentration to half the volume
  6. customon the rotary evaporator, three
  7. washwash steps with saturated NaCl solution
  8. customdrying on sodium sulfate, filtration and reconcentration on the rotary evaporator
  9. customleave as a crude product a yellow oil which
  10. customis purified on silica gel by means of flash column chromatography (flow agent: petroleum ether/ethyl acetate 99:1)