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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358032Generated: November 1, 2026

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

https://huagongshe.com/reaction/2358032

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 numberUS07763639B2
Source datasetuspto-grants-2010_07
ORD IDord-7831ed8929eb4321baedd0a89b6e33e8
Source noteuspto-grants-2010_07