反応 #1766
ord-b4fd402e735143d2ba1df2c8a9a0fe8f
溶媒
反応条件
後処理
- 1ろ過The reaction solution was filtered through celite
- 2workup.DISSOLUTIONThe crude oil was dissolved in EtOAc (1000 mL)
- 3洗浄washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL)
- 4乾燥The EtOAc layer was dried (MgSO4)
- 5ろ過filtered
- 6その他the EtOAc was removed under reduced pressure
- 7その他The crude product was purified by pressurized silica gel column chromatography
- 8その他Evaporation of the hexanes
実験手順
To a stirred, 0° C. solution of methyl 2,4-dihydroxybenzoate (50 g, 300 mmol) in acetone (1000 mL) was added K2CO3 (150 g, 1000 mmol) and benzyl bromide (330 mmol, 39 mL). The solution was allowed to warm to ambient temperature over 48 h. The reaction solution was filtered through celite and the acetone solution stripped down under reduced pressure. The crude oil was dissolved in EtOAc (1000 mL) and washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL). The EtOAc layer was dried (MgSO4), filtered, and the EtOAc was removed under reduced pressure. The crude product was purified by pressurized silica gel column chromatography using 5:1 hexanes:EtOAc. Evaporation of the hexanes:EtOAc mixture gave the desired methyl 4-benzyloxy-2-hydroxybenzoate as a white powder.