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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-fluoro-2-(trifluoromethyl)-HCID 9807—
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-[2-(Trifluoromethyl)phenoxy]-1-azabicyclo[2.2.2]octaneHCID 1019933379%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258392
Source datasetuspto-grants-1993_11
ORD IDord-ec0a81e2fdd044d89fb54e6141d93b73
Source noteuspto-grants-1993_11