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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1199129생성일: 2026년 10월 26일

Diethyl Ether → 6-Fluoro-2,5-dimethylquinoline

https://huagongshe.com/reaction/1199129

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물5-Bromo-6-fluoro-2-methylquinolineHCID 13035313—
반응물HCID 178418332HCID 178418332—
촉매dichloro[1,3-bisdiphenylphosphinopropane] nickel (II)HCID 131716311—
용매TetrahydrofuranHCID 8028—
생성물6-Fluoro-2,5-dimethylquinolineHCID 19868176—

반응 단계

Under a nitrogen atmosphere, 24.0 g (0.1 mole) of 5-bromo-6-fluoro-2-methylquinoline, 2.8 g (0.005 mole) of dichloro[1,3-bisdiphenylphosphinopropane] nickel (II) catalyst, and 380 ml of diethyl ether were combined. 44 ml of 3.17M methylmagnesium chloride in tetrahydrofuran was added dropwise at a rapid rate. The reaction was allowed to stir at room temperature overnight. The ether solution was decanted off into 200 ml of 3N hydrochloric acid in an ice bath, accompanied by vigorous stirring. The aqueous and organic layers were then separated. The aqueous layer was extracted with 100 ml of ethyl acetate and cooled in an ice bath, and the pH was adjusted to pH 10 with concentrated ammonium hydroxide. This was extracted twice with 100 ml of portions of ethyl acetate. The extracts were combined and washed with 30 ml of brine, dried over magnesium sulfate, and filtered and evaporated to give 14.9 g of 2,5-dimethyl-6-fluoroquinoline of 94.4% purity as determined by gas chromatography analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04898945
출처 데이터셋uspto-grants-1990_02
ORD IDord-a4fadf5416a64b4bb709ae26315bbe2f
출처 메모uspto-grants-1990_02