反应详情

To a solution of 7-bromo-2-(4-hydroxy-phenyl)-benzofuran-5-ol 58 (1.0 g, 3.3 mmol) in triethylamine (10 mL) and acetonitrile (10 mL) was added methyl acrylate (0.44 mL, 4.9 mmol) and tri-(o-toly) phosphine (0.2 g, 0.66 mmol). This mixture was purged with nitrogen for 10 minutes. Then palladium (II) acetate (0.037 g, 0.17 mmol) was added and the reaction was heated at reflux for 4 hours; To the cooled reaction was added 2N HCl and the product was extracted into ethyl acetate. The organic layer was washed with brine, dried over MgSO4 and the solvent removed in vacuo. The residue was purified via flash. chromatography on silica gel, eluting with 22–50% ethyl acetate in hexane to give 0.16 g of 59: Mp=231–234° C.; 1HMR (DMSO-d6) δ 9.93 (s, 1 H), 9.44 (s, 1 H), 7.80 (d, 1 H, J=16.1 Hz), 7.72 (d, 2 H, J=8.6 Hz), 7.13 (s, 1 H), 7.02 (d, 1 H, J=2.3 Hz), 6.98 (d, 1 H, J=2.3 Hz), 6.93 (d, 1 H, J=16.2 Hz), 6.92 (d, 2 H, J=8.6 Hz) 3.79 (s, 3 H); MS 311 (M+H)+

1. customThis mixture was purged with nitrogen for 10 minutes
2. temperaturethe reaction was heated
3. temperatureat reflux for 4 hours
4. customTo the cooled reaction
5. extractionthe product was extracted into ethyl acetate
6. washThe organic layer was washed with brine
7. dry with materialdried over MgSO4
8. customthe solvent removed in vacuo
9. customThe residue was purified via flash
10. washchromatography on silica gel, eluting with 22–50% ethyl acetate in hexane