HRID1009160

反应详情

EQUATION

反应方程式

HRID 1009160 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-20 °C

PROCEDURE

实验过程

Methylsulfinyl(methylthio)methane (13 ml, 125 mmol) was dissolved in 250 ml THF and cooled to −20° C. n-Butyllithium (50 ml, 125 mmol) was added and the mixture was stirred for 3 h at −20° C. The mixture was cooled down to −78° C. and a solution of 1-((1,3-dibromopropan-2-yloxy)methyl)benzene (16.000 g, 52 mmol) was added. The reaction was stirred over night and allowed to warm up to RT. It was stirred for an additional 6 h at RT, hydrolyzed with water and extracted with EtOAc. The combined organic extracts were evaporated, dissolved in ether (50 ml) and treated with conc. HCl (10 ml) for 30 min at reflux. The mixture was neutralized with NaOH (10M) and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated. Glass col. Chrom. (10-50% EtOAc in Hex) gave 3-(benzyloxy)cyclobutanone as a yellow oil.

WORKUP

后处理

  1. additionwas added
  2. temperatureThe mixture was cooled down to −78° C.
  3. stirringThe reaction was stirred over night
  4. temperatureto warm up to RT
  5. extractionextracted with EtOAc
  6. customThe combined organic extracts were evaporated
  7. dissolutiondissolved in ether (50 ml)
  8. additiontreated with conc. HCl (10 ml) for 30 min
  9. temperatureat reflux
  10. extractionextracted with EtOAc
  11. dry with materialThe combined organic extracts were dried over MgSO4
  12. customevaporated