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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248752생성일: 2026년 10월 24일

Pyridine → 4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acid

https://huagongshe.com/ko/reaction/248752

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Sodium HydroxideHCID 14798—
반응물4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
반응물4-(Chlorosulfonyl)benzoic acidHCID 82385—
용매DichloromethaneHCID 6344—
생성물4-[N-(4-fluoro-3-trifluoromethylphenyl)sulfamoyl)benzoic acidHCID 3699990—

반응 단계

10 g (55.8 mmol) of 4-fluoro-3-trifluoromethylaniline and 6 ml (74.3 mmol) of pyridine are dissolved in 250 ml of dichloromethane. The mixture is cooled with ice water and, under agitation and exclusion of moisture, 12.7 g (57.6 mmol) of 4-chlorosulfonylbenzoic acid is added in incremental portions. The mixture is stirred overnight; the slurry is combined with 75 ml of 2N sodium hydroxide solution, and the organic phase is separated. The alkaline solution is washed with dichloromethane and then adjusted to pH 2 with hydrochloric acid. The product is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulfate and concentrated to dryness. The title compounds melts at 243-°245° C. after crystallization from ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210290
출처 데이터셋uspto-grants-1993_05
ORD IDord-b639f8a2c482415fbde171d119d57f67
출처 메모uspto-grants-1993_05