Reaktion #725420

ord-5d7fcbe5c86240539394c2771bceaa93

Reaktionsgleichung

[Br][Mg][c]1ccccc1
phenylmagnesium bromide
O=C(CCl)CCl
1,3-dichloroacetone
CC(=O)O
acetic acid
FC(F)(F)C(F)(F)C(F)(F)I
Heptafluoropropyliodide
OC(CCl)(CCl)C(F)(F)C(F)(F)C(F)(F)F
1,3-dichloro-2-(heptafluoropropyl)propan-2-ol

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04560697uspto-grants-1985_12