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HRID 70735作成日:2026年10月25日

Water → 4-Benzyloxybenzophenone

https://huagongshe.com/reaction/70735

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4-HydroxybenzophenoneHCID 14347—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物4-BenzyloxybenzophenoneHCID 458193—

反応手順

NaH (60% in mineral oil, 1.2 g, 30 mmol) was added to an ice-cooled solution of (4-hydroxy-phenyl)-phenyl-methanone (5 g, 25.2 mmol) in DMF (25 mL). Stirred for 20 minutes at room temperature. Benzyl bromide (6.1 ml, 50 mmol) was added at 0° C. The reaction temperature was raised to room temperature after 1 h. Stirred 2 h. Water (20 mL) was added and aqueous phase was extracted dichloromethane (2×30 mL). The combined organic phase was concentrated and purified by flash chromatography (eluent: dichloromethane). 1H nmr revealed the product was pure. Yield: 7.0 g, 96%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822548B2
出典データセットuspto-grants-2014_09
ORD IDord-18532b48adef474fa62a79baa547041c
出典メモuspto-grants-2014_09