HRID1028942

反应详情

EQUATION

反应方程式

HRID 1028942 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

Triflic anhydride (0.18 mL, 1.037 mmol) was added via syringe over 1 min to a stirred mixture of 2-bromo-3-methyl-N-phenethylbenzamide (0.30 g, 0.943 mmol) and 2-chloropyridine (0.11 mL, 1.131 mmol) in DCM (4.7 mL) at −78° C. The reaction mixture was stirred at −78° C. for 5 min, then placed in an ice-water bath and warmed to 0° C. After stirring another 5 min, the solution was allowed to warm to RT and then placed in a pre-heated block and stirred at 45° for 2 h. The reaction mixture was allowed to cool to RT, then it was diluted with 1N NaOH (3 mL) and extracted with DCM (15 mL). The organic extract was washed with saturated aqueous NaCl (2×15 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude material as a light-yellow oil. The crude material was absorbed onto a plug of silica gel and purified by column chromatography eluting with a gradient of 1-10% MeOH/DCM to provide 1-(2-bromo-3-methylphenyl)-3,4-dihydroisoquinoline as off-white glass.

WORKUP

后处理

  1. customplaced in an ice-water bath
  2. temperaturewarmed to 0° C
  3. stirringAfter stirring another 5 min
  4. temperatureto warm to RT
  5. stirringstirred at 45° for 2 h
  6. temperatureto cool to RT
  7. extractionextracted with DCM (15 mL)
  8. extractionThe organic extract
  9. washwas washed with saturated aqueous NaCl (2×15 mL)
  10. dry with materialdried over Na2SO4
  11. filtrationThe solution was filtered
  12. concentrationconcentrated in vacuo
  13. customto give the crude material as a light-yellow oil
  14. customThe crude material was absorbed onto a plug of silica gel
  15. custompurified by column chromatography
  16. washeluting with a gradient of 1-10% MeOH/DCM