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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646110Generated: October 30, 2026

Vanillin → 1-(4'-Hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-one

https://huagongshe.com/reaction/1646110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantHCID 178468789HCID 178468789—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-(4'-Hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-oneHCID 5385892276.5%

Reaction Steps

4-Hydroxy-3-methoxybenzaldehyde (2.1 g, 13.8 mMol) and 3-phenoxypropane-2-one triphenylphosphorane (2.8 g, 6.9 mMol) (prepared as described by LeCorre: C. R. Acad. Sci. Paris, 273 81 (1971)) are dissolved in 100 ml of toluene and warmed to reflux. After three hours, the solvent is evaporated and the residue is taken up in tHF. Sodium bisulfite (10.0 g) is dissolved in 100 ml of water and stirred with the solution for one hour. The THF is evaporated and the water is extracted with chloroform. Drying over magnesium sulfate and evaporation of the chloroform gives a yellow oil. Flash chromatography in ethyl acetate on silica gel gives 1.5 g (65%) of 1-(4'-hydroxy,3'-methoxyphenyl)-4-phenoxy-1-butene-3-one; mp=85°-87° C. C, H analysis: Calcd for C17H16O4 (71.81, 5.68); Found (71.85, 5.50).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05177259
Source datasetuspto-grants-1993_01
ORD IDord-b439e6cd35bc49519ea8039f468cc1f0
Source noteuspto-grants-1993_01