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HRID 422877作成日:2026年10月26日

Water → 4-Benzyloxybenzophenone

https://huagongshe.com/reaction/422877

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). The resulting mixture was stirred for 20 minutes at room temperature (r.t.). Benzyl bromide (6.1 mL, 50 mmol) was added at 0° C. The reaction temperature was raised to r.t. after 1 h and thereafter stirred for additional 2 h. Water (20 mL) was added and the aqueous phase was extracted with dichloromethane (2×30 mL). The combined organic phase was concentrated and purified by flash chromatography (eluent: 100% dichloromethane). Yield: 7.0 g, 96% of 1. 1H NMR (400 MHz, CDCl3): δ 7.83 (d, J=8.4 Hz, 2H), 7.77 (d, J=7.2 Hz, 2H), 7.58-7.52 (m, 1H), 7.50-7.32 (m, 7H), 7.03 (d, J=8.4 Hz, 2H), 5.17 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101651B2
出典データセットuspto-grants-2012_01
ORD IDord-f69a42d30ede4bdf928e670c01543c93
出典メモuspto-grants-2012_01