Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228115Generated: October 30, 2026

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

https://huagongshe.com/reaction/2228115

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 numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-7c4380408a6a4b6ba7873b79acb98bac
Source noteuspto-grants-2002_07