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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612619Generated: November 3, 2026

Acetophenone → 1-Phenyl-3-(4-dimethylaminophenyl)-1-oxo-prop-2-ene

https://huagongshe.com/reaction/1612619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetophenoneHCID 7410—
Reactant4-(Dimethylamino)BenzaldehydeHCID 7479—
ReactantSodium HydroxideHCID 14798—
SolventMethanolHCID 887—
SolventAluminumHCID 5359268—
Product1-Phenyl-3-(4-dimethylaminophenyl)-1-oxo-prop-2-eneHCID 95297—

Reaction Steps

Acetophenone (28.0 g, 0.15 mole) and 4-dimethylaminobenzaldehyde (22.35 g, 0.15 mole) were dissolved in methanol (150 ml) in a 500 ml, 3-necked round bottom flask. The flask was wrapped in aluminium foil to exclude light and was fitted with a mechanical stirrer and a water cooled condenser. The third neck was stoppered and used to obtain samples for monitoring during the reaction. Aqueous sodium hydroxide solution (50 ml of 30% w/v) was added dropwise to the vigorously stirred clear methanolic solution. A yellow/orange solid started separating from the reaction solution (which had turned orange) after about 24 hours. Stirring was continued for about 48 hours at ambient temperature and the intermediate title compound was isolated by vacuum filtration, washed successively with water, methanol and petroleum ether (40-60° C.) and dried in vacuo to give 23.3 g (62% of theory) of 1-phenyl-3-(4-dimethylaminophenyl)-1-oxo-prop-2-ene with a melting point of 112-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190909
Source datasetuspto-grants-1993_03
ORD IDord-389903cbbb2e44af9e2a43173c47ad1c
Source noteuspto-grants-1993_03