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HRID 353049作成日:2026年10月24日

Sodium hydride → 3-(o-Bromobenzyloxy)4-methoxybenzonitrile

https://huagongshe.com/ja/reaction/353049

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Bromobenzyl alcoholHCID 72850—
反応物3-Fluoro-4-methoxybenzonitrileHCID 2774548—
溶媒DimethylformamideHCID 6228—
生成物3-(o-Bromobenzyloxy)4-methoxybenzonitrileHCID 2270701771.4%

反応条件

温度90 °C

反応手順

To a solution of 2-bromobenzyl alcohol (16.50 g, 88.2 mmol) in DMF (100 ml) was added sodium hydride (60% dispersion in mineral oil, 2.94 g, 73.5 mmol) and this was followed by 3-fluoro-4-methoxybenzonitrile (8.88 g, 58.8 mmol) and the resulting mixture was heated to 90° C. for 2 h under N2. After cooling, the mixture was partitioned between ether and H2O, the organic layer washed sequentially with 0.5 N HCl and saturated brine and then dried over MgSO4. Trituration with ether/pentane (1/3, v/v) afforded the subtitle compound as an off-white solid (13.35 g, 71%). Rf 0.27 (hexane/EtOAc 5/1, v/v). MS m/z 318, 320 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750214B2
出典データセットuspto-grants-2004_06
ORD IDord-cf4eb2fcce58450c9e5b5f962b9df908
出典メモuspto-grants-2004_06