Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295227Generated: October 27, 2026

4-Fluorobenzaldehyde → 4-(4-Fluorophenyl)-1,1-diphenyl-3-buten-2-one

https://huagongshe.com/reaction/2295227

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant1,1-DiphenylacetoneHCID 69907—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product4-(4-Fluorophenyl)-1,1-diphenyl-3-buten-2-oneHCID 54147112—

Reaction Steps

A mixture of 4-fluorobenzaldehyde (3.54 gm, 8.5 mmol) and 1,1-diphenylacetone (5.000 gm, 23.8 mmol) in absolute EtOH (50 ml) was treated with a solution of EtONa in EtOH (21% solution, 900 μl, 2.4 mmol). After stirring at room temperature for 22 hours, the mixture was concentrated to 35 ml and the solution was treated with HOAc (200 mg). The solution was cooled to 0° C. and the precipitate that had formed was collected by filtration and washed with cold EtOH. The title compound was obtained as a pale yellow solid (5.787 gm, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691322
Source datasetuspto-grants-1997_11
ORD IDord-615428cd32d9495a9742a44fa551f51f
Source noteuspto-grants-1997_11