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HRID 1670作成日:2026年10月23日

Benzyl Bromide → Methyl 4-(benzyloxy)-2-hydroxybenzoate

https://huagongshe.com/ja/reaction/1670

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物Methyl 2,4-DihydroxybenzoateHCID 16523—
溶媒AcetoneHCID 180—
生成物Methyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726172
出典データセットuspto-grants-1998_03
ORD IDord-b4fd402e735143d2ba1df2c8a9a0fe8f
出典メモuspto-grants-1998_03