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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23543Generated: October 25, 2026

4-Pyridinylacetone → 6-Phenyl-3-(4-pyridinyl)hexa-3,5-dien-2-one

https://huagongshe.com/reaction/23543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinylacetoneHCID 80552—
ReactantCinnamaldehydeHCID 637511—
CatalystAcetic AcidHCID 176—
CatalystPiperidineHCID 8082—
SolventTolueneHCID 1140—
Product6-Phenyl-3-(4-pyridinyl)hexa-3,5-dien-2-oneHCID 5389892617%

Reaction Steps

Trans-cinnamaldehyde (1.84 ml, 14.8 mmol), five drops of piperidine and five drops of acetic acid were added to a solution of 4-pyridyl acetone (2.0 g, 14.8 mmol) in toluene (25 ml). The mixture was heated to reflux for 48 hours with a Dean-Stark trap to remove water. The mixture was concentrated to give a black oil. The oil was purified by silica gel chromatography (eluted with 1:1 hexane/ethyl acetate). The desired fractions were collected, combined and concentrated to give 6-phenyl-3-(4-pyridinyl)hexa-3,5-dien-2-one (628 mg). The ketone was further purified by an additional column chromatography on silica gel (eluting with hexane-ethyl acetate-methylene chloride-methanol (1:1:2:0.12)) (380 mg, 27.3%): Anal. Calc'd for C17H15NO 0.4 H2O: C, 79.91; H, 5.84; N, 5.48. Found: C, 79.72; H, 5.91; N, 5.25. MS (M+H+): 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852740B2
Source datasetuspto-grants-2005_02
ORD IDord-76f21bb7c71f40d295b3b5201fb179c3
Source noteuspto-grants-2005_02