HRID280650

反应详情

EQUATION

反应方程式

HRID 280650 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A stirred, -60° C. solution of 3,5-dichlorotoluene (805 mg, 5.00 mmol) in tetrahydrofuran (5 mL) under nitrogen atmosphere was treated dropwise over 10 minutes with a 1.6M solution of n-butyllithium in hexane (3.3 mL, 5.25 mmol). After addition was complete residual n-butyllithium in the addition funnel was rinsed into the reaction mixture with tetrahydrofuran (1 mL). The reaction mixture was stirred 30 minutes at -55° and then a solution of p-chlorobenzoylchloride (875 mg, 5.00 mmol) in tetrahydrofuran (1.0 mL) was added dropwise over 15 minutes. The mixture was kept at -55° to -30° C. for 2 hours, stirred 2 hours at ambient temperature, and quenched by addition of saturated aqueous ammonium chloride (1.1 mL). After stirring 15 minutes, sodium sulfate (1.1 g) was added, and the mixture was stirred an additional 15 minutes. The solution was decanted, the solids were washed with diethyl ether, and the combined solution and wash were evaporated under reduced pressure. The residue was recrystallized from ethanol (15 mL) to provide 0.78 g (52%) 4-(4-chlorobenzoyl)-3,5-dichlorotoluene.

WORKUP

后处理

  1. additionAfter addition
  2. washwas rinsed into the reaction mixture with tetrahydrofuran (1 mL)
  3. waitThe mixture was kept at -55° to -30° C. for 2 hours
  4. stirringstirred 2 hours at ambient temperature
  5. customquenched by addition of saturated aqueous ammonium chloride (1.1 mL)
  6. stirringAfter stirring 15 minutes
  7. additionsodium sulfate (1.1 g) was added
  8. stirringthe mixture was stirred an additional 15 minutes
  9. customThe solution was decanted
  10. washthe solids were washed with diethyl ether
  11. washthe combined solution and wash
  12. customwere evaporated under reduced pressure
  13. customThe residue was recrystallized from ethanol (15 mL)