Reaction #61356
ord-36cb4228f9774ebfb19b23e47b10f6b2
Reaction equation
Reagents
None
Conditions
Temperature
135°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1Otherfor 16 h
- 2ConcentrationThe solution was concentrated
- 3Otherto afford a brown oil that
- 4ExtractionThe aqueous suspension was extracted twice with ethyl acetate
- 5Washwashed with brine
- 6Dryingdried over MgSO4
- 7Filtrationfiltered
- 8Concentrationconcentrated
- 9Otherchromatographed on silica gel
- 10Washeluting with 3% MeOH in ethyl acetate
Procedure
This amide (250 mg, 1.53 mmol) was refluxed using a Dean-Stark apparatus with aniline (143 mg, 1.53 mmol) and aniline.HCl (10 mg, 0.08 mmol) in toluene (10 mL) for 16 h. The solution was concentrated to afford a brown oil that was mixed with polyphosphoric acid (2 g) and heated at 135° C. for 20 min. The reaction mixture was poured into water and adjusted to pH 8 with 5 M NaOH. The aqueous suspension was extracted twice with ethyl acetate. The organic layers were combined, washed with brine, dried over MgSO4, filtered and concentrated. The residue was flash chromatographed on silica gel, eluting with 3% MeOH in ethyl acetate, to give 2-phenyl-4-hydroxyquinoline (2), 67 mg, 20% yield.