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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101224Generated: October 27, 2026

Methanol → 3-(4-Methoxyphenyl)-1-phenylprop-2-en-1-one

https://huagongshe.com/reaction/2101224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetophenoneHCID 7410—
ReactantSodium HydroxideHCID 14798—
Reactant4-MethoxybenzaldehydeHCID 31244—
SolventEthyl AcetateHCID 8857—
Product3-(4-Methoxyphenyl)-1-phenylprop-2-en-1-oneHCID 94197—

Reaction Steps

Acetophenone (0.5 g) and sodium hydroxide (0.17 g) were suspended in 15 Ml of methanol pre-chilled at −10° C. p-Anisaldehyde (0.57 g) was added thereto, and stirred for 10 hr at room temperature. After neutralization with 5% hydrochloric acid solution, the product was extracted with 100 Ml of ethylacetate. The extracted organic phase was dried with anhydrous magnesium sulfate, and concentrated under vacuum evaporator. Purified compound was obtained by elution with n-hexane:ethylacetate (v/v, 1:7) through silica gel column chromatography (5×3 cm, Merk), and identified as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572831B2
Source datasetuspto-grants-2009_08
ORD IDord-6be23af2371049c49a375372ad07cdd3
Source noteuspto-grants-2009_08