HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,2-Dichloroethane → Ethanone, 1-(4-methoxyphenyl)-2-[3-(trifluoromethyl)phenyl]-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Anisole | HCID 7519 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | 3-(Trifluoromethyl)phenylacetyl chloride | HCID 12751636 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Ethanone, 1-(4-methoxyphenyl)-2-[3-(trifluoromethyl)phenyl]- | HCID 19073195 | — |
Reaktionsschritte
Anisole (32.4 g) and aluminium trichloride (36.0 g) are added to 1,2-dichloroethane (240 ml). The mixture is cooled to -5° and (3-trifluoromethylphenyl)-acetyl chloride (66.8 g) is slowly added. The mixture is stirred for 11/2 hours and poured into a mixture of crushed ice (400 g) and water (150 ml). After heating to room temperature, the compound is extracted with ether (3×200 ml). The combined organic phases are washed with a 2% aqueous solution of sodium hydroxide (200 ml and with water (3×200 ml), dried over magnesium sulphate and the solvents are removed in vacuo. The residue is recrystallised from hexane. The product is dried in vacuo to constant weight to yield 2-(3-trifluoromethylphenyl)-1-(4-methoxyphenyl)-ethanone, m.p. 94°-95°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04818765 |
| Quelldatensatz | uspto-grants-1989_04 |
| ORD ID | ord-8f23000255814d37accaa0726927d36e |
| Quellennotiz | uspto-grants-1989_04 |