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HRID 722408作成日:2026年10月26日

Pyridine → N-(4-fluoro-3-nitrophenyl)benzamide

https://huagongshe.com/reaction/722408

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzoyl chlorideHCID 7412—
反応物4-Fluoro-3-nitroanilineHCID 67768—
溶媒DichloromethaneHCID 6344—
生成物N-(4-fluoro-3-nitrophenyl)benzamideHCID 3535228—

反応条件

温度0 °C

反応手順

To a solution of 4-fluoro-3-nitro aniline (1.00 g, 6.41 mmol) in anhydrous CH2Cl2 (25 ml) was added pyridine (1.52 g, 19.23 mmol) and the solution was cooled to 0° C. under argon. Benzoyl chloride (0.90 g, 6.41 mmol) was added slowly and the solution was then allowed to slowly warm to room temperature and stir for 24 h. The solution was poured into 1NHCl and the organic layer was separated. The aqueous layer was extracted 3× with ethyl acetate (50 ml). The combined organic layers were washed with saturated sodium bicarbonate, water, brine and dried over anhydrous magnesium sulfate. The solution was filtered and the solvent removed under reduced pressure. The residue was purified by flash chromatography, eluting with hexane/ethyl acetate (4:1) to give N-(4-fluoro-3-nitro-phenyl)-benzamide. (1.60 g, 96%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07138420B2
出典データセットuspto-grants-2006_11
ORD IDord-94c691eb4cd04ef2bfa11567dba72890
出典メモuspto-grants-2006_11