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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198735Generated: October 26, 2026

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

https://huagongshe.com/reaction/1198735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHexafluoro-2-butyneHCID 69654—
Reactantp-Chloroacetophenone oximeHCID 96172—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Productp-Chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oximeHCID 131717584—

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281719
Source datasetuspto-grants-1994_01
ORD IDord-9ca5b263c137492bad1e89096fe24021
Source noteuspto-grants-1994_01