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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878941Generated: October 27, 2026

Water → 4-[2-Fluoro-3-(methylsulfonyl)phenyl]-1-propylpiperidine

https://huagongshe.com/reaction/1878941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
Reactant4-[2-Fluoro-3-(methylsulfonyl)phenyl]piperidineHCID 57448038—
SolventAcetonitrileHCID 6342—
Product4-[2-Fluoro-3-(methylsulfonyl)phenyl]-1-propylpiperidineHCID 1151493379.7%

Reaction Steps

To a solution of 4-[2-fluoro-3-(methylsulfonyl)phenyl]piperidine (0.4 g, 1.55 mmol) in acetonitrile (40 ml) was added potassium carbonate (0.3 g, 2.17 mmol) and 1-iodopropane (0.151 ml, 1.55 mmol) and the mixture was heated at reflux for 15 h. The mixture was cooled to ambient temperature and water (50 ml) was added. The aqueous residue was extracted with ethylacetate (3×50 ml) and the combined organic phases was dried, concentrated, and purified by flash column chromatography (ethylacetate/methanol, 1:1) to give the title compound (0.37 g, 79%). The amine was converted to the hydrochloric acid salt and recrystallized from ethanol/diethyl ether: M.p. 255-257° C. MS m/z (relative intensity, 70 eV) 299 (M+, 2), 271 (16), 270 (bp), 147 (9) 133 (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314126B2
Source datasetuspto-grants-2012_11
ORD IDord-e4440f9b7aa0407286abe311330d70de
Source noteuspto-grants-2012_11