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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256578생성일: 2026년 10월 26일

Benzene, 1-fluoro-2-(trifluoromethyl)- → 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane

https://huagongshe.com/reaction/256578

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-fluoro-2-(trifluoromethyl)-HCID 9807—
반응물(+-)-3-QuinuclidinolHCID 15381—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octaneHCID 1019933379%

반응 조건

온도70 °C

반응 단계

A solution of 1.78 g (14 mmol) of 3-quinuclidinol in 20 ml of dry N,N-dimethylformamide (DMF) was added dropwise under nitrogen to a suspension of 0.6 g (15 mmol) of sodium hydride in 20 ml of dry DMF. The mixture was stirred for 15 min at 70° C., and a solution of 3.8 ml (30 mmol) of 2-fluoro-(trifluoromethyl)benzene in 8 ml of dry DMF was added dropwise. The mixture was stirred for another 1.5 h, after which the solvent was evaporated. The residue was dissolved in ethyl acetate and washed with brine. The ethyl acetate layer was separated, dried over magnesium sulfate and evaporated to dryness. The crude compound was purified by column chromatography on silica using methanol-dichloromethane (2:8) as eluent to give 3.0 g (59% yield) of 3-[2-(trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2 ]octane, which was converted into the oxalate salt by treatment with oxalic acid and recrystallization from methanol. m.p. 174° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258392
출처 데이터셋uspto-grants-1993_11
ORD IDord-ec0a81e2fdd044d89fb54e6141d93b73
출처 메모uspto-grants-1993_11