反应 #65919

ord-e48caa78ee5a47feba520d65c2667014

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度ice-cooling
  2. 2
    温度cooling
  3. 3
    过滤The resulting solid was filtered off
  4. 4
    workup.DISTILLATIONthe filtrate was distilled under reduced pressure
  5. 5
    萃取The residue was extracted with 50 ml of chloroform
  6. 6
    洗涤the extract was washed with 1N aqueous sodium hydroxide solution, 1N hydrochloric acid and water in the order
  7. 7
    干燥dried over anhydrous magnesium sulfate
  8. 8
    workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
  9. 9
    其他the residue was purified by silica gel column chromatography

实验过程

In dimethylformamide (50 ml) was dissolved 2-fluoreneacetic acid (2.24 g) followed by addition of 1-hydroxybenztriazole (2.0 g) and, then, dicyclohexylcarbodiimide (3.1 g) with constant stirring and ice-cooling. The mixture was further ,stirred at room temperature for 15 minutes. Cycloheptylamine (1.7 g) was then added under ice-cooling and the mixture was stirred at room temperature for 8 hrs. The resulting solid was filtered off and the filtrate was distilled under reduced pressure. The residue was extracted with 50 ml of chloroform and the extract was washed with 1N aqueous sodium hydroxide solution, 1N hydrochloric acid and water in the order mentioned and dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel column chromatography to give 2.1 g of N-cycloheptyl-2-fluoreneacetamide as a solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05420348uspto-grants-1995_05