HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369783Generated: October 31, 2026
Propanal → (2E)-2-Methyl-3-(3-methylphenyl)-2-propenal
https://huagongshe.com/reaction/2369783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methylbenzaldehyde | HCID 12105 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | (2E)-2-Methyl-3-(3-methylphenyl)-2-propenal | HCID 22157934 | 70% |
Reaction Steps
A solution of potassium hydroxide (24 g, 0.36 mol, 0.6 eq, with a purity of 85%) in ethylene glycol (120 g) and water (12 g) was charged into a 500 mL three-necked round-bottom flask equipped with a reflux condenser and a mechanical stirrer. 3-methyl benzaldehyde (70 g, 0.59 mol) was added dropwise. The stirred reaction mixture was heated at 38-42° C. and propionaldehyde (41 g, 0.71 mol, 1.2 eq) was dosed in over 3.25 h. After a further hour at 40° C., the reaction mixture was cooled to ambient temperature and the two layers separated. The organic layer thus obtained was washed with water (2×100 mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled via a Vigreux column (1.0 mBar, 87-92° C.), to give (2E)-2-methyl-3-(3-methylphenyl)acrylaldehyde (65.9 g, gc purity>95%; yield 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08709994B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-7d5d6fe7d1724e9483a2d243a78968a6 |
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| Source note | uspto-grants-2014_04 |
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