HRID1739783

反应详情

EQUATION

反应方程式

HRID 1739783 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

30 ml (41.7 mmol) of a 1.4 M solution of n-butyllithium in hexane were added dropwise, under a nitrogen atmosphere and at -55° C., to a solution of 6.5 g (41.7 mmol) of bromobenzene in 30 ml of dry THF. After 1 h the solution was allowed to warm up to -20° C. and a solution of 2.4 g (8.3 mmol) of (±)-trans-1,2,3,4,4a,5,6,7,8,8a-decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinone in 20 ml of dry THF was added. The reaction mixture was allowed to warm up to room temperature overnight, then it was quenched with 30 ml of a 5% HCl solution and the phases were separated. The aqueous phase was extracted with AcOEt, then brought to pH 14 with a 2N NaOH solution and extracted with AcOEt. The organic phase was dried over Na2SO4 and the solvent was removed in vacuo. The crude reaction mixture was purified by flash chromatography, eluting with a mixture CH2Cl2 /MeOH/conc. NH4OH 90:7:0.7 respectively, yielding 0.79 g of the title compound.

WORKUP

后处理

  1. temperatureto warm up to room temperature overnight
  2. customit was quenched with 30 ml of a 5% HCl solution
  3. customthe phases were separated
  4. extractionThe aqueous phase was extracted with AcOEt
  5. extractionextracted with AcOEt
  6. dry with materialThe organic phase was dried over Na2SO4
  7. customthe solvent was removed in vacuo
  8. customThe crude reaction mixture
  9. customwas purified by flash chromatography
  10. washeluting with a mixture CH2Cl2 /MeOH/conc