HRID1747689

反应详情

EQUATION

反应方程式

HRID 1747689 的结构方程式

CONDITIONS

反应条件

温度
23 °C

PROCEDURE

实验过程

To a solution of (1R,3S,4S)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanamine (0.098 g, 0.00027 mol) in Methylene chloride (2.0 mL, 0.031 mol) at 0° C. was added triethylamine (0.076 mL, 0.00054 mol) and benzyl chloroformate (0.044 mL, 0.00031 mol). The reaction was warmed to 23° C. overnight. The reaction was quenched by addition of water3 and the mixture was extracted with methylene chloride (3×). The organic layers were washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (0 to 8% EtOAc/hexanes) to obtain 73 mg (54%).

WORKUP

后处理

  1. customThe reaction was quenched by addition of water3
  2. extractionthe mixture was extracted with methylene chloride (3×)
  3. washThe organic layers were washed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified by flash chromatography (0 to 8% EtOAc/hexanes)
  8. customto obtain 73 mg (54%)