Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Epichlorohydrin → 2-Ethoxy-1-methylpyridinium fluoroborate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Epichlorohydrin | HCID 7835 | — |
| 반응물 | Boron trifluoride etherate | HCID 8000 | — |
| 반응물 | 1-Methyl-2(1H)-pyridinone | HCID 12755 | — |
| 반응물 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 생성물 | 2-Ethoxy-1-methylpyridinium fluoroborate | HCID 13059456 | 71% |
반응 단계
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 tetrafluoroborate is dissolved in 20 ml of dry methylene chloride and treated under nitrogen with 4.36 g (0.040 mole) of 1-methyl-2-pyridone in 15 ml of methylene chloride. The reaction mixture is stirred under nitrogen at room temperature overnight (about 16 hours). The solvent is evaporated at room temperature, in vacuo and the quaternary salt obtained is recrystallized from methanol-ether (1:1) to give 8.0 g (71%) of 2-ethoxy-1-methylpyridinium fluoroborate, m.p. 58°-60° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04345083 |
| 출처 데이터셋 | uspto-grants-1982_08 |
| ORD ID | ord-184a5348c3a84a9f84afde24a9c1123e |
| 출처 메모 | uspto-grants-1982_08 |