反应详情

To a solution of (Z)-methyl 2-methoxy-6-((5-oxo-2-phenyloxazol-4(5H)-ylidene)methyl)benzoate (4.2 g, 12.45 mmol) in MeOH (50 mL) was added KOH (2.1 g, 37.35 mmol). The reaction mixture was heated to reflux for 1 hour. The solvent was subsequently removed and the residue was partitioned between water (30 mL) and EtOAc (20 mL). The aqueous layer was extracted with EtOAc (3×20 mL). The organic layers were combined, concentrated in vacuo, adjusted to pH=3 with a 4M solution of HCl in MeOH, and concentrated. The resulting brown solid which was purified by column chromatography eluting with petroleum ether and ethyl acetate (PE/EtOAc=5:1-1:1 gradient) to give the title compound (1 g, 26.3% over 2 steps). 1H NMR (400 MHz, CDCl3) δ ppm 8.55 (s, 1H), 7.58 (t, 1H, J=8.0 Hz), 7.12 (d, 1H, J=8.0 Hz), 6.97 (d, 1H, J=8.0 Hz), 6.67 (s, 1H), 4.01 (s, 3H).

1. temperatureThe reaction mixture was heated
2. temperatureto reflux for 1 hour
3. customThe solvent was subsequently removed
4. customthe residue was partitioned between water (30 mL) and EtOAc (20 mL)
5. extractionThe aqueous layer was extracted with EtOAc (3×20 mL)
6. concentrationconcentrated in vacuo
7. concentrationconcentrated
8. customThe resulting brown solid which was purified by column chromatography
9. washeluting with petroleum ether and ethyl acetate (PE/EtOAc=5:1-1:1 gradient)