HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 2-Ethoxy-1-methylquinolinium fluoroborate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1-Methyl-2-quinolone | HCID 11820 | — |
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Product | 2-Ethoxy-1-methylquinolinium fluoroborate | HCID 13059454 | 83.5% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04266062 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-b35aa481d3e54da7ab217650a0e7c1be |
| Source note | uspto-grants-1981_05 |