HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Epichlorohydrin → 2-Ethoxy-1-methylquinolinium fluoroborate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Epichlorohydrin | HCID 7835 | — |
| Edukt | Boron trifluoride etherate | HCID 8000 | — |
| Edukt | 1-Methyl-2-quinolone | HCID 11820 | — |
| Edukt | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Produkt | 2-Ethoxy-1-methylquinolinium fluoroborate | HCID 13059454 | 83,5% |
Reaktionsschritte
Triethyloxonium fluoroborate is prepared from 3.70 g (0.040 mole) of epichlorohydrin in 14 ml of ether and 7.58 g (0.054 mole) of boron trifluoride etherate in 6 ml of ether. The resulting solid triethyloxonium fluoroborate is dissolved in 20 ml of dry methylene chloride and treated under nitrogen with 6.47 g (0.040 mole) of N-methyl-2-quinolone in 15 ml of methylene chloride. The reaction mixture is stirred under nitrogen at room temperature overnight. The solid is filtered to give 9.2 g (83.5%) of 2-ethoxy-1-methylquinolinium fluoroborate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04345083 |
| Quelldatensatz | uspto-grants-1982_08 |
| ORD ID | ord-cbe2d123b31448a7962b73e59b07b8b2 |
| Quellennotiz | uspto-grants-1982_08 |