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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1-(Methoxymethyl)-alpha-phenyl-alpha-(p-trifluoromethyl-phenyl)imidazole-2-methanol | HCID 12433896 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | alpha-Phenyl-alpha-(p-trifluoromethylphenyl)imidazole-2-methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04152441 |
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| Quelldatensatz | uspto-grants-1979_05 |
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| ORD ID | ord-1f80f93d79a8410a8a6b694a39fa17a8 |
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| Quellennotiz | uspto-grants-1979_05 |
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