HRID451427

反应详情

EQUATION

反应方程式

HRID 451427 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

To a solution of 2,4-dichloro-6-(1-methyl-1-trimethylsilanyloxy-ethyl)-pyrimidine (5.02 g, 18.0 mmol) in THF (60 mL) was added Pd(TPP)4 (0.83 g, 0.72 mmol). The solution was flushed with argon, and subsequently, a 0.5 M solution of 4-chloro-benzylzinc chloride in tetrahydrofuran (36 mL, 18.0 mmol) was added at 20° C. over 1-3 minutes. The reaction mixture was heated to 50° C. for 3 h under an atmosphere of argon. After cooling the mixture to 20° C., saturated aqueous ammonium chloride solution (30 mL) was added to quench the reaction. The mixture was extracted with ethyl acetate (2×30 mL) and the organic layers were washed with brine (2×30 mL), dried over sodium sulfate, and evaporated under reduced pressure. The residual oil was purified by chromatography on silica gel using heptane/0-30% ethyl acetate as eluent to afford the title compound (4.72 g, 71%) as a colorless oil.

WORKUP

后处理

  1. customThe solution was flushed with argon
  2. temperatureAfter cooling the mixture to 20° C.
  3. customto quench
  4. customthe reaction
  5. extractionThe mixture was extracted with ethyl acetate (2×30 mL)
  6. washthe organic layers were washed with brine (2×30 mL)
  7. dry with materialdried over sodium sulfate
  8. customevaporated under reduced pressure
  9. customThe residual oil was purified by chromatography on silica gel