Fluorobenzene → 3-Chloro-1-(4-fluorophenyl)-2-methylpropan-1-one

HRID 918289

Reaktionsgleichung

Reaktionsgleichung von HRID 918289
[Cl-].[Al+3].[Cl-].[Cl-].[F:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cl:12][CH2:13][CH:14]([CH3:18])[C:15](Cl)=[O:16]>>[Cl:12][CH2:13][CH:14]([CH3:18])[C:15]([C:9]1[CH:10]=[CH:11][C:6]([F:5])=[CH:7][CH:8]=1)=[O:16]

Komponenten

4

Versuchsvorschrift

To a slurry of 22.7 g. (0.17 mole) of anhydrous aluminum chloride and 9.6 g. (0.10 mole) of fluorobenzene is added 14.1 g. (0.10 mole) of β-chloroisobutyrylchloride over 30 minutes at 20° to 25°C. The mixture is aged for 30 minutes at 20° to 25°C and then quenched in ice. The product is extracted into hexane. The hexane layer is dried over anhydrous sodium sulfate and concentrated in vacuo to give 3-chloro-4'-fluoro-2-methylpropiophenone.

Aufarbeitung

  1. customquenched in ice
  2. extractionThe product is extracted into hexane
  3. dry with materialThe hexane layer is dried over anhydrous sodium sulfate
  4. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-4c423730beba48a7a4ec648a407851e8
Quelldatensatz
uspto-grants-1976_07
Patentnummer
US03970693

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