反应详情

温度

80 °C

A mixture of 2-benzyloxyphenylboronic acid (20.2 g, 88.6 mmol), methyl 2-bromo-5-nitrobenzoate (25.4 g, 97.5 mmol), cesium carbonate (57.7 g, 177 mmol) and bis(triphenylphosphine)palladium(II) dichloride (1.16 g, 1.65 mmol) was suspended in anhydrous N,N-dimethylformamide (300 mL), and then was stirred under argon atmosphere at 80° C. for 3 days. After cooling down, ethyl acetate (500 mL), diethylether (300 mL) and water (500 mL) were added thereto, and then separated. The aqueous layer was extracted with a mixture of ethyl acetate (200 mL) and diethylether (200 mL). The combined organic layer was washed with water (500 mL, twice) and saturated brine (300 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (21.0 g) as a pale yellow oil. (Yield 65%)

1. temperatureAfter cooling down
2. customseparated
3. extractionThe aqueous layer was extracted with a mixture of ethyl acetate (200 mL) and diethylether (200 mL)
4. washThe combined organic layer was washed with water (500 mL
5. dry with materialtwice) and saturated brine (300 mL) successively, dried over anhydrous magnesium sulfate
6. customthe solvent was removed under reduced pressure
7. customThe obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate)