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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67180생성일: 2026년 10월 24일

Epichlorohydrin → 2-Ethoxy-1-methylquinolinium fluoroborate

https://huagongshe.com/ko/reaction/67180

반응식

참여 물질

역할이름HCID투입량
반응물EpichlorohydrinHCID 7835—
반응물Boron trifluoride etherateHCID 8000—
반응물1-Methyl-2-quinoloneHCID 11820—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물Triethyloxonium tetrafluoroborateHCID 2723982—
생성물2-Ethoxy-1-methylquinolinium fluoroborateHCID 1305945483.5%

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 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04345083
출처 데이터셋uspto-grants-1982_08
ORD IDord-cbe2d123b31448a7962b73e59b07b8b2
출처 메모uspto-grants-1982_08