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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55980생성일: 2026년 10월 24일

Water → N-[2-(3,5-dichloropyridin-2-yl)-2-(ethoxyimino)ethyl]-2-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/55980

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
반응물2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-O-ethyloximeHCID 118071516—
용매DichloromethaneHCID 6344—
생성물N-[2-(3,5-dichloropyridin-2-yl)-2-(ethoxyimino)ethyl]-2-(trifluoromethyl)benzamideHCID 13173688356.1%

반응 단계

To a solution of 200 mg of 2-amino-1-(3,5-dichloropyridin-2-yl)ethanone-β-ethyloxime and 90 mg of triethylamine in 3 ml of dichloromethane, 169 mg of 2-(trifluoromethyl)benzoyl chloride was added dropwise with stirring under cooling with ice, and after the addition, the mixture was stirred at room temperature for another 30 minutes. After completion of the reaction, the reaction mixture was mixed with 10 ml of water and extracted with ethyl acetate (15 ml×1), the resulting organic layer was washed with water (10 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 1:9 to 3:7) as the eluent to obtain 190 mg of the desired product as a pale yellow resinous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434684B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-9054a357c6634b4abced56e566dacb4b
출처 메모uspto-grants-2016_09