Reaktion #2379298

ord-dd0f3f7f89dd490d8e6657a5e44a1ef5

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschen, then washed with aqueous ammonium chloride solution (20% w/v 2×100 ml)
  2. 2
    ExtraktionThe aqueous phase was extracted with ether (2×100 ml)
  3. 3
    Trocknenthe combined ether layers were dried (magnesium sulphate)
  4. 4
    Sonstigeevaporated in vacuo
  5. 5
    Sonstigeto give an oil
  6. 6
    Sonstigewas removed from the product by distillation in vacuo (80°-90°/10-15 mm Hg)
  7. 7
    SonstigeA portion of the residue was crystallised from industrial methylated spirit

Vorschrift

Quinoline (40 g) was dissolved in dry ether (250 ml) and treated dropwise with a solution of phenyl lithium (160 ml of 1.88 m solution in benzene/ether). The mixture was stirred at room temperature for 18 hr., then washed with aqueous ammonium chloride solution (20% w/v 2×100 ml) and then water (2×100 ml). The aqueous phase was extracted with ether (2×100 ml) and the combined ether layers were dried (magnesium sulphate) and evaporated in vacuo to give an oil. Unreacted quinoline was removed from the product by distillation in vacuo (80°-90°/10-15 mm Hg). A portion of the residue was crystallised from industrial methylated spirit to afford 2-phenylquinoline m.pt. 84°-86° characterised by its nmr spectrum. The bulk of the product was also characterised by its nmr spectrum.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04801593uspto-grants-1989_01