Reaktion #1475722

ord-a4c90e2160364c8da612467ed4e2d9bf

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITto stand overnight
  2. 2
    SonstigeThe aqueous layer is then separated
  3. 3
    Waschenthe organic layer washed with water
  4. 4
    Trocknena 5% sodium hydroxide solution, dried with magnesium sulfate
  5. 5
    Sonstigeevaporated
  6. 6
    workup.DISTILLATIONThe residue is distilled in vacuo

Vorschrift

Triethylbenzylammonium chloride (3.6 g) is added to a solution of 39.9 g of crude 2-chloro-5-(trifluoromethylthio) benzyl alcohol in 400 ml of dichloromethane and the mixture is treated dropwise at 15°-20° C. with a solution of 20.6 g of potassium dichromate in 270 ml of water containing 135 ml of sulfuric acid. The mixture is stirred for 4 hours at room temperature and allowed to stand overnight. The aqueous layer is then separated and the organic layer washed with water and a 5% sodium hydroxide solution, dried with magnesium sulfate and evaporated. The residue is distilled in vacuo. There are obtained 34.1 g of crude 2-chloro-5-(trifluoromethylthio)benzaldehyde boiling at 120°-130° C./2 kPa. According to the 1H-NMR spectrum the product consists of approximately 80% of the named compound and the remainder is the position isomer. In this state the substance is suitable for further processing.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04431808uspto-grants-1984_02