HRID1517239

反应详情

EQUATION

反应方程式

HRID 1517239 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

Ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate (67 mmol) was dissolved in THF (900 mL) to give a yellow solution. The mixture was cooled in a −78° C. bath under nitrogen atmosphere (internal temp. about −70° C.). DIBAL-H (1 M in THF; 200 mmol) was added over 45 min. via syringe. The reaction was warmed to −60° C. after the addition, and then allowed to warm slowly to 0° C. over night. The reaction was quenched by slow addition of saturated aqueous ammonium chloride (200 mL). The mixture was then warmed to room temperature. Ether (400 mL) and saturated aqueous sodium potassium tartrate (200 mL) were added. The mixture was stirred vigorously for 30 min. After separation of the layers, the aqueous layer was extracted with ether and the combined organics washed with brine, dried with sodium sulfate, filtered and concentrated under vacuum to give (4-chloro-2-(methylthio)pyrimidin-5-yl)methanol as a solid (84%).

WORKUP

后处理

  1. customto give a yellow solution
  2. temperatureThe reaction was warmed to −60° C.
  3. additionafter the addition
  4. temperatureto warm slowly to 0° C. over night
  5. customThe reaction was quenched by slow addition of saturated aqueous ammonium chloride (200 mL)
  6. temperatureThe mixture was then warmed to room temperature
  7. additionEther (400 mL) and saturated aqueous sodium potassium tartrate (200 mL) were added
  8. customAfter separation of the layers
  9. extractionthe aqueous layer was extracted with ether
  10. washthe combined organics washed with brine
  11. dry with materialdried with sodium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated under vacuum