HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018467Generated: October 26, 2026
4-Methoxybenzaldehyde → p-METHOXY-alpha-METHYLCINNAMALDEHYDE
https://huagongshe.com/reaction/1018467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | 2-(Triphenylphosphoranylidene)propionaldehyde | HCID 4280987 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | p-METHOXY-alpha-METHYLCINNAMALDEHYDE | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482824B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-4fea7ee6dbb645a8bf40f2145fab96eb |
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| Source note | uspto-grants-2002_11 |
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