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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720736Generated: October 27, 2026

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

https://huagongshe.com/reaction/1720736

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, 28.5 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 numberUS05506219
Source datasetuspto-grants-1996_04
ORD IDord-4672aafb982e44a6bb1801223e5321bf
Source noteuspto-grants-1996_04