HRID12922

反应详情

EQUATION

反应方程式

HRID 12922 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a 15 mL of anhydrous DMF was added NaH (60% dispersion in oil, 338 mg, 8.44 mmol), and the resulting reaction mixture was cooled to 0° C. p-benzyloxy phenol (1.41 g, 7.03 mmol) was added and the reaction mixture was stirred at rt for 45 min. It was then cooled to −5° C., and (R)-Boc-prolinol tosylate (2.5 g, 7.03 mmol) in anhydrous DMF (5 mL) was cooled in a separate ice-bath and added dropwise to the reaction mixture. It was then allowed to warm to rt and stirred at 92° C. for 5 h and at rt overnight. The resulting mixture was poured into 200 mL ice/water and stirred for an hour. The resulting precipitate was filtered, washed with ether, dried over MgSO4, concentrated, recrystallized with ether/hexane to give shiny yellow crystals (1.5 g, 55%).

WORKUP

后处理

  1. customthe resulting reaction mixture
  2. additionwas added
  3. temperatureIt was then cooled to −5° C.
  4. additionadded dropwise to the reaction mixture
  5. temperatureto warm to rt
  6. stirringstirred at 92° C. for 5 h and at rt overnight
  7. stirringstirred for an hour
  8. filtrationThe resulting precipitate was filtered
  9. washwashed with ether
  10. dry with materialdried over MgSO4
  11. concentrationconcentrated
  12. customrecrystallized with ether/hexane