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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484231생성일: 2026년 10월 23일

Methanol → p-Chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oxime

https://huagongshe.com/ko/reaction/484231

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Hexafluoro-2-butyneHCID 69654—
반응물p-Chloroacetophenone oximeHCID 96172—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
생성물p-Chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oximeHCID 131717584—

반응 단계

Hexafluoro-2-butyne is slowly bubbled through a 55°-60° C. solution of p-chloroacetophenone oxime (17.0 g, 0.10 mol), methanol (80 mL) and potassium tert-butoxide (1.12 g, 0.01 mol) over a 5 hour period. The solvent is removed in vacuo to obtain a liquid which is poured into water and extracted with ether. The combined organic extracts are washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give an oil. The oil is chromatographed using silica gel and eluted with 1% ethylacetate in methylene chloride to 5% ethyl acetate in methylene chloride to give p-chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oxime, vinyl-(Z) as a yellow liquid (21.5 g, 65%) and 2-(p-chlorophenyl)-4,5-trans-bis(trifluoromethyl)-1-pyrrolin-5-ol as a white solid (2.35 g, mp 152.5°-153° C., 7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05229524
출처 데이터셋uspto-grants-1993_07
ORD IDord-8d5d1b80327f474fac12a48de13f6ca9
출처 메모uspto-grants-1993_07