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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70813생성일: 2026년 10월 23일

Trifluoroacetic anhydride → 2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxide

https://huagongshe.com/ko/reaction/70813

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Carbamide PeroxideHCID 31294—
반응물2-Cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamideHCID 86672971—
용매DichloromethaneHCID 6344—
생성물2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxideHCID 8667297081%

반응 단계

2-Cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide (240 mg) was dissolved in dichloromethane, added with urea-hydrogen peroxide adduct (85 mg) and trifluoroacetic anhydride (190 mg), and stirred at room temperature for 20 hours. The reaction solution was concentrated under the reduced pressure, and the resulting residues were dissolved in ethyl acetate. The solution was washed with water and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the solvent was removed by distillation under the reduced pressure. The resulting residues were purified by column chromatography to obtain 2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxide (0.20 g, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822691B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-df3e9f22808e44b8a724cb76231ba676
출처 메모uspto-grants-2014_09