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HRID 1198735作成日:2026年10月27日

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

https://huagongshe.com/reaction/1198735

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Hexafluoro-2-butyneHCID 69654—
反応物p-Chloroacetophenone oximeHCID 96172—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
生成物p-Chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oximeHCID 131717584—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05281719
出典データセットuspto-grants-1994_01
ORD IDord-9ca5b263c137492bad1e89096fe24021
出典メモuspto-grants-1994_01