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HRID 1030986作成日:2026年10月26日

Water → N-(2,5-Difluoro-4-nitrophenyl)acetamide

https://huagongshe.com/reaction/1030986

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Acetic AnhydrideHCID 7918—
反応物2,5-Difluoro-4-nitroanilineHCID 235930—
触媒Sulfuric AcidHCID 1118—
触媒2-DimethylaminopyridineHCID 21885—
溶媒DichloromethaneHCID 6344—
生成物N-(2,5-Difluoro-4-nitrophenyl)acetamideHCID 1462489388.4%

反応手順

A mixture of 6.0 g (0.034 mole) of 2,5-difluoro-4-nitroaniline, 6.5 g (0.064 mole) of acetic anhydride, and approximately 0.1 g (0.0008 mole) of dimethylaminopyridine in 300 ml of methylene chloride was stirred and heated at reflux for two hours. The reaction mixture was allowed to cool and stir at room temperature for approximately 18 hours. The solvent was removed from the mixture by distillation under reduced pressure, leaving a residue. To this residue was added 32.5 g (0.318 mole) of acetic anhydride and several drops of concentrated sulfuric acid. This mixture was stirred at room temperature for approximately 18 hours. Approximately 300 ml of water was added to the mixture causing a vigorous exotherm and a solid to form. This solid was collected by filtration. The filter cake was washed with water and was dried under reduced pressure to yield 6.5 g of N-(2,5-difluoro-4-nitrophenyl)acetamide. The nmr spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05108486
出典データセットuspto-grants-1992_04
ORD IDord-e03af009080341838c315f5351746e77
出典メモuspto-grants-1992_04