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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387850Generated: November 1, 2026

Ethanol → 1-(4-(3-(4-Fluoro-phenyl)cinnamoylamino)benzyl)piperidine

https://huagongshe.com/reaction/1387850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-(3-Bromocinnamoylamino)benzyl)piperidineHCID 53907766—
Reactant4-Fluorophenyl borateHCID 86756158—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product1-(4-(3-(4-Fluoro-phenyl)cinnamoylamino)benzyl)piperidineHCID 5396777192.8%

Reaction Steps

A suspension of 1-(4-(3-bromocinnamoylamino)-benzyl)piperidine (0.4 g), 4-fluorophenyl borate (0.14 g), 1M potassium carbonate (2 ml) and ethanol (1 ml) in toluene (5 ml) was stirred under argon atmosphere at room temperature for 30 minutes. To the suspension was added tetrakistriphenylphosphinepalladium (0.05 g), and the mixture was refluxed over night. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column (methanol/triethylamine/ethyl acetate) to give crude crystals, which were recrystallized from ethyl acetate-hexane to give 1-(4-(3-(4-fluoro-phenyl)-cinnamoylamino)benzyl)piperidine (Compound 83) (0.35 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-40afed8c837d4106b8e390e8e3219135
Source noteuspto-grants-2001_07