Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484231Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktHexafluoro-2-butyneHCID 69654—
Eduktp-Chloroacetophenone oximeHCID 96172—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
Produktp-Chloro-0-[1,2-bis(trifluoromethyl)vinyl]acetophenone oximeHCID 131717584—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05229524
Quelldatensatzuspto-grants-1993_07
ORD IDord-8d5d1b80327f474fac12a48de13f6ca9
Quellennotizuspto-grants-1993_07