HRID1613935

反应详情

EQUATION

反应方程式

HRID 1613935 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

0.29 ml of a hexane solution of 0.48 mmols of n-butyl lithium was added to a solution of 218 mg (0.48 mmols) of octyltriphenylphosphonium bromide in 3 ml of tetrahydrofuran and stirred at room temperature for 5 minutes. This solution was cooled to -78° C., after which 1.43 g (8 mmols) of hexamethylphosphorus triamide was added and stirred for 5 minutes, followed by further addition of 2 ml of a tetrahydrofuran solution of 98.8 mg (0.40 mmols) of 2-formyl-3-methyl-4-acetoxy-6-fluoroquinoline and stirring at -78° C. for 15 minutes and -42° C. for 30 minutes. The reaction solution was added to 20 ml of water and extracted with ethyl acetate, followed by washing with a saturated sodium chloride aqueous solution and drying with anhydrous sodium sulfate. After removal of the solvent by distillation under reduced pressure, the residue was purified by silica gel column chromatography (solvent n-hexane ethyl acetate=30:1 ) to obtain 14 mg (yield 10 %) of 2-(trans-1-nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline.

WORKUP

后处理

  1. temperatureThis solution was cooled to -78° C.
  2. stirringstirred for 5 minutes
  3. stirringstirring at -78° C. for 15 minutes and -42° C. for 30 minutes
  4. extractionextracted with ethyl acetate
  5. washby washing with a saturated sodium chloride aqueous solution
  6. dry with materialdrying with anhydrous sodium sulfate
  7. customAfter removal of the solvent
  8. distillationby distillation under reduced pressure
  9. customthe residue was purified by silica gel column chromatography (solvent n-hexane ethyl acetate=30:1 )