HRID2246748

反应详情

EQUATION

反应方程式

HRID 2246748 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

A reaction flask (500 mL) containing zinc chloride (6.98 g, 51.2 mmol) was dried by heating using a heat gun under vacuum. After cooling to room temperature, a solution of 3-chloro-5-fluorophenylmagnesium bromide (0.5 M in dry tetrahydrofuran, 100 mL, 50.0 mmol) was added to the reaction flask via a cannula, and the mixture was stirred until all zinc chloride solid was dissolved and the formation of a sluggish bright yellow solution (˜1 h). A warm bath (40° C.) may be applied to complete this process. Anhydrous tetrahydrofuran (100 mL) was added, followed by tetrakis(triphenylphosphine)palladium (2.89 g, 2.50 mmol, 0.05 equiv.). After cooling to 0° C., 3-chloropropionyl chloride (5.05 mL, 52.5 mmol, 1.05 equiv.) was added dropwise and the mixture was stirred at 0° C. for 2 h. The reaction mixture was acidified with an aqueous hydrochloric acid solution (3N), then extracted with diethyl ether (2×250 mL). The combined ether extracts were washed with a saturated aqueous sodium bicarbonate solution, brine, dried (anhydrous sodium sulfate), and concentrated. The crude oil was purified by Isco CombiFlash Companion column chromatography (silica gel, 0-15% ethyl acetate/hexane) and the resulting white solid was recrystallized (minimal diethyl ether/hexane/−25° C.) to give pure 3-chloro-1-(3-chloro-5-fluorophenyl)propan-1-one as a white powder. Yield: 5.54 g (50%).

WORKUP

后处理

  1. customwas dried
  2. temperatureby heating
  3. dissolutionwas dissolved
  4. customthe formation of a sluggish bright yellow solution (˜1 h)
  5. customA warm bath (40° C.) may be applied
  6. temperatureAfter cooling to 0° C.
  7. extractionextracted with diethyl ether (2×250 mL)
  8. washThe combined ether extracts were washed with a saturated aqueous sodium bicarbonate solution, brine
  9. dry with materialdried (anhydrous sodium sulfate)
  10. concentrationconcentrated
  11. customThe crude oil was purified by Isco CombiFlash Companion column chromatography (silica gel, 0-15% ethyl acetate/hexane)
  12. customthe resulting white solid was recrystallized (minimal diethyl ether/hexane/−25° C.)