HRID1267737

反应详情

EQUATION

反应方程式

HRID 1267737 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-30 °C

PROCEDURE

实验过程

5,5,6,6,6-Pentafluorohexanoic acid (95 g, 460.92 mmol) was dissolved in anhydrous tetrahydrofuran (1L) and cooled to −30° C. To this solution, borane-methyl sulfide complex (10 M in THF, 92.2 ml, 921.84 mmol) was slowly added dropwise, followed by stirring for 3 hours at room temperature. After treatment with methanol at 0° C., water was added to the reaction mixture, which was then extracted twice with ether. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the resulting residue was dissolved in dichloromethane (1500 ml), and triethylamine (160.6 ml, 1.15 mol) and methanesulfonyl chloride (46.4 ml, 599.19 mmol) were added dropwise thereto at 0° C., followed by stirring for 1 hour. After the reaction was completed, water was added to the reaction mixture, which was then extracted twice with dichloromethane. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4) to give 1-methanesulfonyloxy-5,5,6,6,6-pentafluorohexane (101 g, Yield 81%).

WORKUP

后处理

  1. extractionwas then extracted twice with ether
  2. washThe combined organic layers were washed with water and saturated aqueous sodium chloride
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationAfter distilling off the solvent
  5. dissolutionthe resulting residue was dissolved in dichloromethane (1500 ml)
  6. customat 0° C.
  7. stirringby stirring for 1 hour
  8. extractionwas then extracted twice with dichloromethane
  9. washThe combined organic layers were washed with water and saturated aqueous sodium chloride
  10. dry with materialdried over anhydrous magnesium sulfate
  11. distillationAfter distilling off the solvent
  12. customthe residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4)