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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018467Generated: October 26, 2026

4-Methoxybenzaldehyde → p-METHOXY-alpha-METHYLCINNAMALDEHYDE

https://huagongshe.com/reaction/1018467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant2-(Triphenylphosphoranylidene)propionaldehydeHCID 4280987—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Productp-METHOXY-alpha-METHYLCINNAMALDEHYDEHCID 228993—

Reaction Steps

A suspension of 4-methoxybenzaldehyde (10 g, 0.073 mol) and α-formylethylidenetriphenylphosphorane (25.7 g, 0.081 mol) in dried toluene (200 ml)was heated with stirring at reflux under an atmosphere of nitrogen for 24 h. The cooled reaction mixture was decanted to removed insoluble material and evaporated to give a brown oil. The oil was taken up in diethylether and the resulting suspension purified on flash silica eluting with hexane-diethyl ether (3:2). The resulting oil was a mixture of required product and 4-methoxybenzaldehyde and therefore dissolved in dried toluene (150 ml) and reaction continued as described above with α-formylethylidenetriphenylphosphorane (5.76 g, 0.018 ml) for 7 h. Following the work up and chromatography as above 3-(4-methoxyphenyl)-2-methylpropenaldehyde was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482824B1
Source datasetuspto-grants-2002_11
ORD IDord-4fea7ee6dbb645a8bf40f2145fab96eb
Source noteuspto-grants-2002_11