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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033186생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1033186

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Acetic AnhydrideHCID 7918—
반응물2,5-Difluoro-4-nitroanilineHCID 235930—
촉매Sulfuric AcidHCID 1118—
촉매2-DimethylaminopyridineHCID 21885—
용매DichloromethaneHCID 6344—
생성물N-(2,5-Difluoro-4-nitrophenyl)acetamideHCID 1462489388.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310724
출처 데이터셋uspto-grants-1994_05
ORD IDord-577bd73ef8644ddb9ec7a279ccfeae41
출처 메모uspto-grants-1994_05