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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880484Generated: October 30, 2026

Piperidine → 1-(2-Fluoro-4-nitrophenyl)piperidine

https://huagongshe.com/reaction/880484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventAcetonitrileHCID 6342—
Product1-(2-Fluoro-4-nitrophenyl)piperidineHCID 1070434592.3%

Reaction Steps

Piperidine (0.80 g, 9.42 mmol) was added to a solution of 3,4-difluoro-nitro benzene (1.0 g, 6.28 mmol) in acetonitrile (15 mL) and diisopropyl ethylamine (1.62 g, 12.57 mmol) and the mixture was refluxed for 3 h. The acetonitrile was removed in vacuo and the residue was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over anhydrous sodium sulphate and concentrated in vacuo to afford 1-(2-fluoro-4-nitro-phenyl)piperidine (1.3 g, 92%) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993574B2
Source datasetuspto-grants-2015_03
ORD IDord-7e425c5665d7458a8ebddabc6ccd6988
Source noteuspto-grants-2015_03