Reaktion #2379299
ord-3a38e7a0aac74c86b363628340687700
Reaktionsgleichung
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturheated
- 2workup.ADDITIONwas added in portions over 1 hr
- 3TemperaturThe resulting mixture was maintained
- 4Temperaturat reflux for a further 3 hr
- 5SonstigeThe alcohol was removed in vacuo
- 6ExtraktionThe resulting solution was extracted with ether (4×150 ml)
- 7Trocknenthe ether layer was dried (magnesium sulphate)
- 8Sonstigeevaporated in vacuo
- 9Sonstigeto give an oil which
- 10workup.DISTILLATIONwas distilled twice
Vorschrift
2-Phenylquinoline (65 g) was dissolved in absolute alcohol (200 ml) and heated to reflux when sodium metal (25 g) was added in portions over 1 hr. The resulting mixture was maintained at reflux for a further 3 hr. The mixture was diluted with water (300 ml) and acidified with conc. hydrochloric acid. The alcohol was removed in vacuo and the residue made basic with 10M sodium hydroxide solution. The resulting solution was extracted with ether (4×150 ml) and the ether layer was dried (magnesium sulphate) and evaporated in vacuo to give an oil which was distilled twice to give the product, 1,2,3,4-tetrahydro-2-phenylquinoline (b.pt. 114°/0.1 mm Hg). This was characterised by its nmr spectrum.