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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230327Generated: October 26, 2026

Piperidine → 4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one

https://huagongshe.com/reaction/2230327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
Reactant4-PyridinylacetoneHCID 80552—
SolventTolueneHCID 1140—
Product4-(3-Fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-oneHCID 69373148393.2%

Reaction Steps

A solution of 4-pyridylacetone (1.0 g, 7.4 mmol), 3-fluoro-p-anisaldehyde (1.25 g, 8.1 mmol), and piperidine (0.13 g, 1.5 mmol) in toluene (50 ml) was heated to reflux. After 18 hours, the reaction was cooled to room temperature and the solvent was removed under reduced pressure. The crude product (3.0 g) was purified by column chromatography (silica gel, 65:35 ethyl acetate/hexane) to give 4-(3-fluoro-4-methoxylphenyl)-3-pyridyl-3-butene-2-one as a pale yellow solid (1.60 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423713B1
Source datasetuspto-grants-2002_07
ORD IDord-0a713c33112c43b6b5e23afbba76168b
Source noteuspto-grants-2002_07