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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489921Generated: October 25, 2026

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

https://huagongshe.com/reaction/489921

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 numberUS06979686B1
Source datasetuspto-grants-2005_12
ORD IDord-f9ced75ef53c4362afa8e12efbbe0011
Source noteuspto-grants-2005_12