HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256578Generated: October 25, 2026
Benzene, 1-fluoro-2-(trifluoromethyl)- → 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane
https://huagongshe.com/reaction/256578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene, 1-fluoro-2-(trifluoromethyl)- | HCID 9807 | — |
| Reactant | (+-)-3-Quinuclidinol | HCID 15381 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octane | HCID 10199333 | 79% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258392 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-ec0a81e2fdd044d89fb54e6141d93b73 |
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| Source note | uspto-grants-1993_11 |
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