Reaktion #2379298
ord-dd0f3f7f89dd490d8e6657a5e44a1ef5
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Waschen, then washed with aqueous ammonium chloride solution (20% w/v 2×100 ml)
- 2ExtraktionThe aqueous phase was extracted with ether (2×100 ml)
- 3Trocknenthe combined ether layers were dried (magnesium sulphate)
- 4Sonstigeevaporated in vacuo
- 5Sonstigeto give an oil
- 6Sonstigewas removed from the product by distillation in vacuo (80°-90°/10-15 mm Hg)
- 7SonstigeA 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.