HRID1966167

反应详情

EQUATION

反应方程式

HRID 1966167 反应方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a stirred solution of 1-(3-[tert-butyl(diphenyl)silyl]oxycyclobutyl)ethanone (0.65 g, 0.0018 mol) in dichloromethane (10 mL) at 0° C. was added sodium bicarbonate (0.39 g, 0.0046 mol) and m-chloroperbenzoic acid (1.0 g, 0.0046 mol) with stirring. The reaction was stirred at rt over night. LCMS showed incomplete reaction, another 2.5 eq. of mCPBA and NaHCO3 were added and the reaction was stirred for another day. The reaction was quenched with 20% aq. Na2S2O3 solution (50 mL) and stirred for a further 30 min at rt, then extracted with dichloromethane. The combined organic layers were washed with brine, dried over MgSO4, concentrated and purified on silica gel with Combiflash (silica gel, 0-10% EtOAc/Hex) to give the desired product (0.3 g, 40%) as colorless oil. LCMS calculated for C22H29O3Si(M+H)+: 369.2. Found: 369.4.

WORKUP

后处理

  1. stirringThe reaction was stirred at rt over night
  2. customreaction
  3. stirringthe reaction was stirred for another day
  4. customThe reaction was quenched with 20% aq. Na2S2O3 solution (50 mL)
  5. stirringstirred for a further 30 min at rt
  6. extractionextracted with dichloromethane
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. custompurified on silica gel with Combiflash (silica gel, 0-10% EtOAc/Hex)