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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085401Generated: October 31, 2026

Potassium Carbonate → 3-[4-(4-Fluorophenyl)piperidin-1-yl]propylphthalimide

https://huagongshe.com/reaction/2085401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluoro-phenyl)-piperidine hydrochlorideHCID 21898168—
ReactantBromopropylphthalimideHCID 21958088—
SolventDimethylformamideHCID 6228—
Product3-[4-(4-Fluorophenyl)piperidin-1-yl]propylphthalimideHCID 2272947311.8%

Reaction Conditions

Temperature97.5 °C

Reaction Steps

A mixture of 4-(4-fluorophenyl)piperidine hydrochloride (5.08 g, 23.2 mmol), 3-bromopropylphthalimide (6.22 g, 23.2 mmol), and potassium carbonate (15 g) in DMF (100 mL) was stirred at 95-100° C. for 12 h. About 80% of the solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate (200 mL) and washed with brine (3×100 mL) and dried (Na2SO4). The solvent was evaporated from the ethyl acetate solution and the residue was purified by column chromatography (1/1 hexane-ethyl acetate to 100% ethyl acetate), giving crude product (7.50 g, 88%). This crude product was crystallized from isopropanol, giving a white crystalline solid (4.50 g, 1st crop). This material was used in the next step. Concentration of the mother liquor and cooling gave the second crop of desired product (1.0 g). 1H NMR δ 1.43-1.52 (m, 2H), 1.67-1.75 (m, 2H), 1.80-1.96 (m, 4H), 2.33-2.46 (m, 3H), 2.94-2.99 (br d, 2H), 3.78 (t, J=7 Hz, 2H), 6.90-7.04 (m, 4H), 7.70-7.74 (m, 2H), 7.84-7.87 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720324B2
Source datasetuspto-grants-2004_04
ORD IDord-72e485f20b0345cc969056e77e1cd75f
Source noteuspto-grants-2004_04