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HRID 478612作成日:2026年10月27日

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

https://huagongshe.com/reaction/478612

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 0.5N 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US06642242B2
出典データセットuspto-grants-2003_11
ORD IDord-37301b24540e494493599c8b813ae6cb
出典メモuspto-grants-2003_11