反应 #725420

ord-5d7fcbe5c86240539394c2771bceaa93

反应条件

温度
-20°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONWhen this addition
  2. 2
    workup.ADDITIONTo this solution was added, at -78° C.
  3. 3
    其他the temperature below -65° C
  4. 4
    workup.STIRRINGThe mixture was then stirred four hours between -20° and -50° C
  5. 5
    温度to warm to 5° C.
  6. 6
    其他the phases were separated
  7. 7
    洗涤The aqueous phase was washed with ether (2×25 ml)
  8. 8
    干燥dried (MgSO4)
  9. 9
    其他evaporated

实验过程

Heptafluoropropyliodide (5 g, 6.9 mmole) was stirred at -78° C. in dry diethylether (20 ml). A solution of phenylmagnesium bromide in ethyl ether (10 ml of a 1.88 M solution) was added over a half-hour period. When this addition was complete, the reaction mixture was stirred at -20° C. for one hour. To this solution was added, at -78° C., 1,3-dichloroacetone (3.25 g, 25.6 mmole) in dry diethylether (20 ml) dropwise, keeping the temperature below -65° C. The mixture was then stirred four hours between -20° and -50° C. Glacial acetic acid (3 ml) in diethylether (5 ml) was added slowly followed by water (15 ml). The mixture was allowed to warm to 5° C. and then the phases were separated. The aqueous phase was washed with ether (2×25 ml). The ethereal extracts were combined, dried (MgSO4) and evaporated to give crude 1,3-dichloro-2-(heptafluoropropyl)propan-2-ol, which was used directly in the next step.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04560697uspto-grants-1985_12