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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518680Generated: October 27, 2026

Potassium Iodide → 1-(2-(3-Fluoro-4-nitrophenoxy)ethyl)piperidine

https://huagongshe.com/reaction/518680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
ReactantPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
Reactant3-Fluoro-4-nitrophenolHCID 520948—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(2-(3-Fluoro-4-nitrophenoxy)ethyl)piperidineHCID 66728447—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-fluoro-4-nitrophenol (3.07 g, 19.54 mmol), 1-(2-chloroethyl)piperidine hydrochloride (3.60 g, 19.54 mmol), cesium carbonate (19.10 g, 58.6 mmol) and potassium iodide (1.622 g, 9.77 mmol) were combined with DMF (19.54 mL), and the mixture was heated at 50° C. for 36 hours. The resulting mixture was diluted with EtOAc (50 mL), washed with water (100 mL) and the water layer extracted with EtOAc (30 mL). The combined organic layers were washed with water (20 mL×2), 1N aqueous NaOH, and brine, and the organic layer was dried over Na2SO4, filtered and evaporated. The residue was purified via flash chromatography using a linear gradient of 0% to 5% of 1% NH4OH in MeOH in DCM. The title compound was isolated as a yellow liquid (662 mg, 13% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-c6c5f94887d846b78e49d77e8361971e
Source noteuspto-grants-2015_08