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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197661Generated: November 2, 2026

3-Nitrobenzaldehyde → 4-(3-Nitrophenyl)-3-(4-pyridyl)-3-butene-2-one

https://huagongshe.com/reaction/1197661

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant4-PyridinylacetoneHCID 80552—
ReactantPiperidinium acetateHCID 3014295—
SolventBenzeneHCID 241—
Product4-(3-Nitrophenyl)-3-(4-pyridyl)-3-butene-2-oneHCID 54510285—

Reaction Steps

4.62 g (34 mmole) of 1-(4-pyridyl)-2-propanone and 5.14 g (34 mmol) of 3-nitrobenzaldehyde were dissolved in benzene. To this solution, 0.49 g (3.4 mmol) of piperidinium acetate was added, and the mixture was refluxed with application of heat for 6 hours for dehydration. The reaction mixture was washed with water, and dried over anhydrous sodium sulfate. The benzene contained in the reaction mixture was distilled off under reduced pressure and the remaining reaction product was chromatographed on a silica gel column, whereby the captioned compound was obtained. The yield was 7.695 g (87.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276150
Source datasetuspto-grants-1994_01
ORD IDord-3830e8a8ca094c8093f1cf9791e37998
Source noteuspto-grants-1994_01