HRID1027678

反应详情

EQUATION

反应方程式

HRID 1027678 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

Lithium diisopropyl amide (16.9 mL, 1.5 M in cyclohexane, 25.4 mmol) was added to THF (40 mL) at −78° C. A solution of 4-picoline (2.50 mL, 25.4 mmol) in THF (30.0 mL) was added dropwise to the LDA solution. The dry ice bath was removed. The reaction mixture was stirred at 0° C. for 30 minutes, and cooled down to −78° C. A solution of N-methoxy-N-methylbenzamide (1) (5.00 g, 29.6 mmol) in THF (20.0 mL) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. The mixture was quenched with water, and extracted with ethyl acetate (3×). The pooled organic layer was dried over magnesium sulfate. The mixture was filtered, and the solvent was removed under vacuum to give the crude product. The crude material was triturated with hot hexane, and filtered to give 1-phenyl-2-(pyridin-4-yl) ethanone (2) as a yellow solid (3.53 g, 17.9 mmol, 70% yield).

WORKUP

后处理

  1. customThe dry ice bath was removed
  2. temperaturecooled down to −78° C
  3. temperatureThe reaction mixture was warmed to room temperature
  4. stirringstirred overnight
  5. customThe mixture was quenched with water
  6. extractionextracted with ethyl acetate (3×)
  7. dry with materialThe pooled organic layer was dried over magnesium sulfate
  8. filtrationThe mixture was filtered
  9. customthe solvent was removed under vacuum
  10. customto give the crude product
  11. customThe crude material was triturated with hot hexane
  12. filtrationfiltered