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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228041Generated: October 30, 2026

Water → 1-[2-(4-Nitrophenyl)ethyl]piperidine

https://huagongshe.com/reaction/2228041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Nitrophenethyl bromideHCID 79266—
SolventDimethylformamideHCID 6228—
Product1-[2-(4-Nitrophenyl)ethyl]piperidineHCID 220573—

Reaction Conditions

Temperature70 °C

Reaction Steps

In DMF (100 ml) was dissolved 4—(2-bromoethyl)nitro-benzene (25.0 g), and to the solution were added piperidine (12.9 ml) and potassium carbonate (18.0 g). The mixture was stirred at 70° C. for 15 hours, and to the mixture was added water (900 ml), and then the mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate) to give 1-[2—(4-nitro-phenyl)ethyl]piperidine (24.8 g) as orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-ade00f285a1d494b9c5c58e4c3ef3105
Source noteuspto-grants-2002_07