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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720735Generated: November 1, 2026

Sulfuric Acid → 3-(4-Fluorophenyl)-1-phenylprop-2-en-1-one

https://huagongshe.com/reaction/1720735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetophenoneHCID 7410—
ReactantSodium HydroxideHCID 14798—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-(4-Fluorophenyl)-1-phenylprop-2-en-1-oneHCID 9820160.1%

Reaction Steps

A mixture of acetophenone (7.02 gm, 58.4 mmol), p-fluorobenzaldehyde (7.24 gm, 58.4 mmol) and concentrated H2SO4 (10 ml) in glacial HOAc (116 ml) was stirred at room temperature for 2 days. The solution was poured into H2O (250 ml) and neutralized with 10% NaOH (200 ml). The aqueous layer was extracted once with Et2O and the Et2O layer was washed successively with H2O, saturated NaHCO3 (twice) and brine, then dried (magnesium sulfate). Filtration and removal of the solvent afforded a yellow solid, which was recrystallized from hot hexane to give the title compound (7.94 gm, 60%) as light yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506219
Source datasetuspto-grants-1996_04
ORD IDord-165e5704582e4858a3180791eaf90df1
Source noteuspto-grants-1996_04