戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 50869作成日:2026年10月24日

Sodium hydride → (E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazole

https://huagongshe.com/ja/reaction/50869

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-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
反応物2-[(E)-2-phenylethenyl]-1H-benzimidazoleHCID 5708003—
触媒CopperHCID 23978—
溶媒DimethylacetamideHCID 31374—
生成物(E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazoleHCID 227366475%

反応条件

温度0 °C

反応手順

To a stirred solution of (E)-2-styryl-1H-benzimidazole (0.49 g, 2.2 mmol) in dimethylacetamide (20 ml) at 0° C. under a nitrogen atmosphere was added sodium hydride (0.11 g, 2.8 mmol). After stirring at 0° C. for 20 min. and then at room temperature for 30 min., a solution of 2-Chloro-3-trifluoromethylpyridine (0.60 g, 3.3 mmol) in dimethylacetamide (5 ml) was added. The resulting mixture was heated to reflux for about 3 h 20 min. After cooling, copper bronze (0.45 g, 7.1 mg-atom) was added and heating was continued for 9 h 20 min. The reaction mixture was filtered through a pad of celite and the filtrate was diluted with dichloromethane (200 ml), washed consecutively with water (3×200 ml) and brine (100 ml), dried (magnesium sulfate) and concentrated to dryness. Purification by column chromatography (silica gel, 150 g; n-hexane/ethyl acetate (2/1)) followed by recrystallization from a mixture of isopropyl ether and n-hexane yielded 37 mg (5%) of the titled compound as white solids. MW: 365.36; mp: 156.0-157.0° C.; 1H-NMR (CDCl3) δ: 8.96 (1H, dd, J=4.8, 1.8 Hz), 8.36 (1H, dd, J=8.1, 1.8 Hz), 7.90 (1H, d, J=15.8 Hz), 7.84 (1H, d, J=8.1 Hz), 7.76 (1H, d, J=8.1, 4.8 Hz), 7.45-7.20 (7H, m), 6.92 (1H, d, J=7.7 Hz), 6.47 (1H, d, J=15.8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713482B2
出典データセットuspto-grants-2004_03
ORD IDord-61cef2dd26354f48a48b428e9f443eab
出典メモuspto-grants-2004_03