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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261948Erstellt: 25. Oktober 2026

Acetic Acid → alpha-Phenyl-alpha-(p-trifluoromethylphenyl)imidazole-2-methanol

https://huagongshe.com/reaction/261948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
Edukt1-(Methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanolHCID 12433896—
LösungsmittelWaterHCID 962—
Produktalpha-Phenyl-alpha-(p-trifluoromethylphenyl)imidazole-2-methanolHCID 12433853—

Reaktionsschritte

A mixture of 9 g. (0.025 mol) of 1-(methoxymethyl)-α-phenyl-α-(p-trifluoromethyl-phenyl)imidazole-2-methanol, 70 ml. of glacial acetic acid, 7 ml. of concentrated hydrochloric acid and 7 ml. of water was refluxed for 3.5 hours. After cooling, the liquid was distilled off and 2 N sodium hydroxide solution and a small amount of ethanol were added to the residue. The alcohol was distilled off and the aqueous phase was extracted with diethyl ether. The ethereal solution was washed with water and dried over sodium sulphate and the solvent was distilled off. The residue was first crystallised from a mixture of toluene and petroleum ether (boiling range 40°-60° C.) and subsequently from isopropyl alcohol. α-Phenyl-α-(p-trifluoromethylphenyl)imidazole-2-methanol was obtained. Melting point 174°-175.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152441
Quelldatensatzuspto-grants-1979_05
ORD IDord-1f80f93d79a8410a8a6b694a39fa17a8
Quellennotizuspto-grants-1979_05