HRID378380

反应详情

EQUATION

反应方程式

HRID 378380 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

1.0 g of ethyl (E)-3-[1-(1-methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]-2-butenoate prepared in Example 1 was dissolved in 20 ml of tetrahydrofuran. The obtained solution was cooled to -70° C., followed by the gradual addition of 7.0 ml (10.5 mmol) of a 1.5M solution of diisobutylaluminum hydride in toluene. The obtained mixture was stirred for 2 hours, followed by the addition of an aqueous solution of ammonium chloride. The obtained mixture was extracted with ethyl acetate. The organic phase was washed with a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated in a vacuum to give 650 mg of the title compound as a colorless oil.

WORKUP

后处理

  1. extractionThe obtained mixture was extracted with ethyl acetate
  2. washThe organic phase was washed with a saturated aqueous solution of common salt
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated in a vacuum