HRID1920867

反应详情

EQUATION

反应方程式

HRID 1920867 的结构方程式

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

2-[3-(3-Bromophenyl)oxetan-3-yl]acetic acid (840 mg, 2.789 mmol) was dissolved in tert-butanol (8 mL) and triethylamine (310.5 mg, 427.7 μL, 3.068 mmol) was added followed by diphenylphosphoryl azide (844.3 mg, 661.2 μL, 3.068 mmol). Heat at 80° C. for 4 hours. The reaction was allowed to cool and the solvent removed under reduced pressure. Ethyl acetate was added and the organic layer was washed with 5% citric acid soln, NaHCO3 (sat. aq. soln.) and brine. The organics were dried over MgSO4, filtered and the solvent removed under reduced pressure. The crude product was pre-adsorbed onto silica and purified (Companion, 40 g) eluting with 2.5-50% EtOAc:Petrol ether to give tert-butyl N-[[3-(3-bromophenyl)oxetan-3-yl]methyl]carbamate as a white solid (433 mg, 45%).

WORKUP

后处理

  1. temperatureto cool
  2. customthe solvent removed under reduced pressure
  3. additionEthyl acetate was added
  4. washthe organic layer was washed with 5% citric acid soln
  5. dry with materialThe organics were dried over MgSO4
  6. filtrationfiltered
  7. customthe solvent removed under reduced pressure
  8. custompurified (Companion, 40 g)
  9. washeluting with 2.5-50% EtOAc