HRID1444697

反应详情

EQUATION

反应方程式

HRID 1444697 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 1-(7-bromo-3,4-dihydroisoquinolin-2(1H)-yl)-2,2,2-trifluoroethanone (5.34 g, 17.3 mmol) and Pd(dppf)Cl2.CH2Cl2 (708 mg, 0.867 mmol) was azeotroped with benzene and suspended in 50 mL of dry THF. At room temperature, 4-ethoxy-4-oxobutylzinc bromide (0.5M in THF, 52 mL, 26 mmol) was added dropwise with syringe. The orange suspension became a clear brown solution. The reaction mixture was then refluxed for 2 h. After cooling to room temperature, it was quenched with brine, extracted with EtOAc, washed with 10% HCl and brine, dried over Na2SO4, and evaporated to dryness. Flash chomatography (SiO2, EtOAc/hexane=15:100 to 20:100) gave ethyl 4-(2-(2,2,2-trifluoroacetyl)-1,2,3,4-tetrahydroisoquinolin-7-yl)butanoate as a white solid.

WORKUP

后处理

  1. temperatureThe reaction mixture was then refluxed for 2 h
  2. customit was quenched with brine
  3. extractionextracted with EtOAc
  4. washwashed with 10% HCl and brine
  5. dry with materialdried over Na2SO4
  6. customevaporated to dryness