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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856018Generated: October 29, 2026

Sodium Iodide → 1-[2-(Tetrahydropyran-2-yloxy)ethyl]-4-(4-trifluoromethylphenoxy)piperidine

https://huagongshe.com/reaction/856018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
Reactant4-(4-(Trifluoromethyl)phenoxy)piperidineHCID 3688392—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-[2-(Tetrahydropyran-2-yloxy)ethyl]-4-(4-trifluoromethylphenoxy)piperidineHCID 2308133959.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(4-trifluoromethylphenoxy)-piperidine (1.87 g, 7.63 mmol), 2-(2-bromoethoxy)-tetrahydropyran (1.75 g, 8.4 mmol), potassium carbonate (1.16 g, 8.38 mmol), sodium iodide (1.2 g, 8.01 mmol) in DMF (30 ml) was stirred at 100° C. for 1 hour. The reaction mixture was allowed to return to room temperature, poured into water and extracted with ethyl acetate twice. The extract was washed with water twice and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/methanol=50/1) to afford 1-[2-(tetrahydropyran-2-yloxy)ethyl]-4-(4-trifluoromethylphenoxy)piperidine (1.69 g, yield 59%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-5150eea560c240e2a9fbdc981192b314
Source noteuspto-grants-2007_08