Reaktion #710430

ord-d1e9bf383cb44af58c0c5606de4f61e3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was refluxed for 1 hr
  2. 2
    TemperaturAfter cooling
  3. 3
    Temperaturcooling
  4. 4
    workup.STIRRINGstirred at 100° C. on an oil bath for 30 min
  5. 5
    TemperaturAfter cooling
  6. 6
    Extraktionthe reaction solution was extracted with methylene chloride
  7. 7
    Waschenwashed with water
  8. 8
    Trocknendried over anhydrous magnesium sulfate
  9. 9
    SonstigeThe residue was chromatographed on a column of silica gel
  10. 10
    EinengenThe eluate with 10% acetonitrile-methylene chloride was concentrated
  11. 11
    Sonstigethe product was recrystallized from acetone-ether

Vorschrift

To 5.4 ml of a solution of 2.04M of boron trichloride in toluene was added a solution of 1.67 g of carbazole in 10 ml of toluene, and the mixture was refluxed for 1 hr. After cooling, the mixture was treated with 1 ml of methyl thiocyanate and stirred at room temperature for 3 hr. The reaction mixture was poured into 4N aqueous sodium hydroxide under ice-cooling and stirred at 100° C. on an oil bath for 30 min. After cooling, the reaction solution was extracted with methylene chloride, washed with water and dried over anhydrous magnesium sulfate. The residue was chromatographed on a column of silica gel, and the eluate with methylene chloride was discarded. The eluate with 10% acetonitrile-methylene chloride was concentrated, and the product was recrystallized from acetone-ether to give 1.45 g of 1-cyanocarbazole as white crystals melting at 200°-201° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04774331uspto-grants-1988_09