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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56056생성일: 2026년 10월 23일

Water → N-[2-[3-chloro-5-(3,3-dimethyl-1-butynyl)pyridin-2-yl]-2-(isopropoxyimino)ethyl]-2-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/56056

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3,3-Dimethyl-1-butyneHCID 13512—
반응물N-[2-(5-bromo-3-chloropyridin-2-yl)-2-(isopropoxyimino)ethyl]-2-(trifluoromethyl)benzamideHCID 131736909—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TriethylamineHCID 8471—
생성물N-[2-[3-chloro-5-(3,3-dimethyl-1-butynyl)pyridin-2-yl]-2-(isopropoxyimino)ethyl]-2-(trifluoromethyl)benzamideHCID 13173691099.7%

반응 조건

온도80 °C

반응 단계

To a solution of 0.15 g of N-[2-(5-bromo-3-chloropyridin-2-yl)-2-(isopropoxyimino)ethyl]-2-(trifluoromethyl)benzamide and 0.05 g of 3,3-dimethyl-1-butyne in 3 ml of triethylamine, 0.04 g of copper(I) iodide and 0.02 g of dichlorobistriphenylphosphine palladium(II) were added, and the mixture was stirred at 80° C. for 3 hours. After completion of the reaction, the reaction mixture was allowed to cool to room temperature, mixed with 10 ml of water and extracted with ethyl acetate (20 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 residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 1:5 to 2:4) as the eluent to obtain 0.15 g of the desired product as a yellow resinous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434684B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-18bcfc0220ed4658b8e7553f85be4284
출처 메모uspto-grants-2016_09