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HRID 850454作成日:2026年10月25日

Water → 3-Benzyloxyphenylacetonitrile

https://huagongshe.com/reaction/850454

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物2-(3-Hydroxyphenyl)acetonitrileHCID 13781042—
溶媒DimethylformamideHCID 6228—
生成物3-BenzyloxyphenylacetonitrileHCID 51983186.8%

反応条件

温度90 °C

反応手順

3-Hydroxyphenylacetonitrile (834 mg, 6.26 mmol) was dissolved in DMF (10 ml), and to this solution were successively added benzyl bromide (0.82 ml, 6.89 mmol, 1.1 eq) and anhydrous potassium carbonate (1.30 g, 9.40 mmol, 1.5 eq). The mixture was stirred under heating at 90° C. for 1.5 hours. This reaction mixture was cooled to room temperature, and water (20 ml) was added. The mixture was extracted twice with ethyl acetate (40 ml). The organic layers were combined, washed with saturated brine (80 ml) and dried over anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (hexane/ethyl acetate=1/1) to give (3-benzyloxyphenyl)acetonitrile (1.21 g, 86.8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06017919
出典データセットuspto-grants-2000_01
ORD IDord-014b240ba2084d1681e8d47222a0e1e9
出典メモuspto-grants-2000_01