HRID465754

反应详情

EQUATION

反应方程式

HRID 465754 的结构方程式

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

A mixture of 2.09 g (9.5 mmol) of 1-benzoyloxy-3-hydroxymethyl-2-methylenecyclobutane from Step G, 112 mL of methylene chloride and 28 mL of methanol was cooled to -78° C. under a nitrogen atmosphere. Ozone was bubbled through the mixture for 10 minutes, until a persistent blue color was observed. Excess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide was added and the reaction mixture stirred for 0.5 h at -78° C. The reaction mixture was allowed to warm to ambient temperature, stirred for 0.5 h at ambient temperature and evaporated under reduced pressure to a syrup. The syrup (2.5 g) was dissolved to ~2 mL of methylene chloride and purified on a 1.5×45 cm silica gel column eluted @5 psi with 100 mL of methylene chloride, followed by 250 mL of 1% methanol in methylene chloride and 250 mL of 2% methanol in methylene chloride to give 1.79 g (86% yield) of the title compound; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.

WORKUP

后处理

  1. customOzone was bubbled through the mixture for 10 minutes, until a persistent blue color
  2. customExcess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide
  3. additionwas added
  4. temperatureto warm to ambient temperature
  5. stirringstirred for 0.5 h at ambient temperature
  6. customevaporated under reduced pressure to a syrup
  7. dissolutionThe syrup (2.5 g) was dissolved to ~2 mL of methylene chloride
  8. custompurified on a 1.5×45 cm silica gel column
  9. washeluted @5 psi with 100 mL of methylene chloride