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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70805생성일: 2026년 10월 24일

Water → N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]quinoline-6-carboxamide

https://huagongshe.com/ko/reaction/70805

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물4-(1,1,1,2,3,3,3-Heptafluoropropan-2-yl)-2,6-dimethylanilineHCID 9882425—
용매DichloromethaneHCID 6344—
생성물N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]quinoline-6-carboxamideHCID 8667296378%

반응 단계

Quinoline-6-carboxylic acid (1.0 g) was dissolved in dichloromethane. N,N-dimethylformamide (300 μL) and oxalyl chloride (1.2 g) were added to this solution at room temperature and stirred for two hours followed by reflux for 20 minutes. The solvent was removed under the reduced pressure, and quinoline-6-carbonyl chloride was obtained as a crude product, which was then dissolved in dichloromethane. To this solution, 4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylaniline (1.6 g) dissolved in dichloromethane and pyridine (1.2 g) were added and stirred at room temperature for 5 hours. The reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined and washed with 1N hydrochloric acid and water, and dried over anhydrous magnesium sulfate. The drying agent (anhydrous magnesium sulfate) was removed by filtration and the solvent was distilled off under the reduced pressure. The residue was purified by column chromatography to obtain N-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2,6-dimethylphenyl]quinoline-6-carboxamide (2.0 g, yield 78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822691B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d855bb5b0d594f0cac7ac30fbe15706e
출처 메모uspto-grants-2014_09