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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058004Generated: October 26, 2026

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

https://huagongshe.com/reaction/1058004

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 numberUS06514977B1
Source datasetuspto-grants-2003_02
ORD IDord-ec1d28fe36db49a2905b1e46f1a76b87
Source noteuspto-grants-2003_02