HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Carbon Dioxide → HCID 178444273, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Trifluoroacetyl chloride | HCID 61106 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | HCID 178444253 | HCID 178444253 | — |
| Lösungsmittel | HCID 178503046 | HCID 178503046 | — |
| Produkt | HCID 178444273 | HCID 178444273 | — |
Reaktionsschritte
0.5 mol of 4-(trans-4-pentylcyclohexyl)biphenyl, 500 ml of carbon sulfide and 0.5 mol of aluminium chloride are introduced into a three-neck flask fitted with a dry-ice reflux condenser. After the mixture has been cooled to -30°, 0.5 mol of trifluoroacetyl chloride are condensed in. The mixture is then allowed to warm to 0° and stirred at this temperature for 6 hours then at room temperature for 14 hours. The reaction mixture is poured onto a mixture of ice and dilute hydrochloric acid. The organic phase is separated off, and the aqueous phase is extracted by shaking with dichloromethane (2×50 ml). The organic phases are combined, the solvents removed by distillation and the product is recrystallized twice from ethanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05045229 |
| Quelldatensatz | uspto-grants-1991_09 |
| ORD ID | ord-fc0f90bcff1744139f0b48dc85ae1ad1 |
| Quellennotiz | uspto-grants-1991_09 |