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HRID 51298作成日:2026年10月25日

Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/reaction/51298

反応式

関与物質

役割名称HCID仕込み量
反応物Phenethyl bromideHCID 7666—
反応物Sodium hydrideHCID 24758—
反応物1H-Imidazole-4-carbaldehydeHCID 76428—
溶媒TetrahydrofuranHCID 8028—
生成物1-Phenethyl-1H-imidazole-4-carbaldehydeHCID 22289872—

反応手順

Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713496B2
出典データセットuspto-grants-2004_03
ORD IDord-31441750fe72498fa9d8520b043eb1a1
出典メモuspto-grants-2004_03