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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67179생성일: 2026년 10월 25일

Epichlorohydrin → 2-Ethoxy-1-methylpyridinium fluoroborate

https://huagongshe.com/reaction/67179

반응식

참여 물질

역할이름HCID투입량
반응물EpichlorohydrinHCID 7835—
반응물Boron trifluoride etherateHCID 8000—
반응물1-Methyl-2(1H)-pyridinoneHCID 12755—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물Triethyloxonium tetrafluoroborateHCID 2723982—
생성물2-Ethoxy-1-methylpyridinium fluoroborateHCID 1305945671%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04345083
출처 데이터셋uspto-grants-1982_08
ORD IDord-184a5348c3a84a9f84afde24a9c1123e
출처 메모uspto-grants-1982_08