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HRID 253455作成日:2026年10月27日

Dimethylformamide → 4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehyde

https://huagongshe.com/reaction/253455

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物2-Chloro-4-hydroxy-5-methoxybenzaldehydeHCID 29000—
反応物4-(1H-benzoimidazol-2-ylmethoxy)-5-chloro-2-fluoro-benzaldehydeHCID 59803854—
生成物4-(1H-benzoimidazol-2-ylmethoxy)-2-chloro-5-methoxy-benzaldehydeHCID 59803890—

反応条件

温度80 °C

反応手順

2-Chloro-4-hydroxy-5-methoxy-benzaldehyde (136, 2.30 g, 0.0123 mol) was dissolved in N,N-dimethylformamide (89.5 mL, 1.16 mol) and sodium hydride (60% dispersion in mineral oil, 541 mg, 0.0135 mol) was added. After 20 minutes, 2-chloromethyl-1H-benzoimidazole (106, 2.05 g, 0.0123 mol) was added to the reaction. The reaction was stirred at 80° C. overnight. The reaction was concentrated in vacuo to an oil. Ethyl acetate was added and washed with saturated sodium bicarbonate and brine. The organic layer was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with 30-70% ethyl acetate in hexane over 30 minutes to provide a white solid (137, 1.79 g, 46%). MS (ESI) [M+H+]+=317.1, 319.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872018B2
出典データセットuspto-grants-2011_01
ORD IDord-fc39b84c238541d1868b16b5ef595e9e
出典メモuspto-grants-2011_01