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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene, 1-fluoro-2-(trifluoromethyl)- | HCID 9807 | — |
| 반응물 | (+-)-3-Quinuclidinol | HCID 15381 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane | HCID 10199333 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05258392 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-ec0a81e2fdd044d89fb54e6141d93b73 |
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| 출처 메모 | uspto-grants-1993_11 |
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