HRID984722

反应详情

EQUATION

反应方程式

HRID 984722 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

An oven dried Schlenk tube equipped with a rubber septum was cooled under an argon urge. The septum was removed and the tube was charged with palladium acetate (5.6 mg, 0.025 mmol, 5 mol % Pd), (±)-BINAP (23.3 mg, 0.0375 mmol, 7.5 mol %) and 2-methyl-5-(N-methyl-anilinomethylene)-cyclopentanone (108 mg, 0.5 mmol). Toluene (2 mL) was added and the mixture was stirred for 1 min at 40° C. 4-t-Butylbromobenzene (0.17 mL, 1.0 mmol) and sodium t-butoxide (96 mg, 1.0 mmol) were added to the tube, the tube was capped with the septum, purged with argon, and additional toluene (4 mL) was added through the septum. The mixture was heated to 100° C. with stirring until the starting ketone had been completely consumed as judged by GC analysis. The mixture was cooled to room temperature, quenched with saturated aqueous ammonium chloride (10 mL) and diluted with ether (20 mL). The mixture was poured into a separatory funnel and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel to afford 116 mg (67%) of the title compound.

WORKUP

后处理

  1. customAn oven dried Schlenk tube
  2. customequipped with a rubber septum
  3. temperaturewas cooled under an argon urge
  4. customThe septum was removed
  5. customthe tube was capped with the septum
  6. custompurged with argon, and additional toluene (4 mL)
  7. additionwas added through the septum
  8. temperatureThe mixture was heated to 100° C.
  9. stirringwith stirring until the starting ketone
  10. customhad been completely consumed
  11. temperatureThe mixture was cooled to room temperature
  12. customquenched with saturated aqueous ammonium chloride (10 mL)
  13. additiondiluted with ether (20 mL)
  14. additionThe mixture was poured into a separatory funnel
  15. customthe layers were separated
  16. extractionThe aqueous layer was extracted with ether (20 mL)
  17. washthe combined organic layers were washed with brine (20 mL)
  18. dry with materialdried over anhydrous magnesium sulfate
  19. filtrationfiltered
  20. concentrationconcentrated in vacuo
  21. customThe crude material was purified by flash chromatography on silica gel