HRID1796265

反应详情

EQUATION

反应方程式

HRID 1796265 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

(2R,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(3-fluoro-2′-methylsulfanyl-biphenyl-4-ylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (4.1 g, 7.3 mmol) was dissolved in 20 mL EtOAc, added added m-chloroperoxybenzoic acid (7.2 g, 29 mmol) in one portion and stirred at ambient temperature for 3 hours. A 10% aqueous solution (50 mL) of Na2S2O3 was added to the vigorously stirring reaction in order to quench peroxide. After 20 minutes the solution was diluted with 100 mL EtOAc, separated layers, washed organics with sat. NaHCO3 (3×100 mL), water (2×100 mL), brine, dried with MgSO4, filtered and concentrated to yield title compound. (4.3 g, 99%) APCI (AP−): 591.3 (M−H)−.

WORKUP

后处理

  1. additionadded
  2. stirringvigorously stirring
  3. customreaction in order
  4. customto quench peroxide
  5. additionAfter 20 minutes the solution was diluted with 100 mL EtOAc
  6. customseparated layers
  7. washwashed organics with sat. NaHCO3 (3×100 mL), water (2×100 mL), brine
  8. dry with materialdried with MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated