HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439614Generated: October 30, 2026
Benzaldehyde → (E)-3-methoxycarbonyl-4-phenyl-3-butenoic acid methyl ester
https://huagongshe.com/reaction/439614
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Dimethyl Succinate | HCID 7820 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | (E)-3-methoxycarbonyl-4-phenyl-3-butenoic acid methyl ester | HCID 6186590 | 66.1% |
Reaction Steps
To a solution of potassium t-butoxide (16.8 g) in t-butyl alcohol (150 ml) is added dropwise with stirring a solution of benzaldehyde (15.9 g) and succinic acid dimethyl ester (26.3 g) in t-butyl alcohol (20 ml) at room temperature, and the mixture is stirred for 30 minutes. The reaction mixture is poured into ice-water (200 ml), and the mixture is extracted with isopropyl ether. The pH value of the aqueous layer is adjusted to pH 2-3, and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed, dried, and evaporated to remove the solvent. The residue is dissolved in methanol (75 ml), and thereto is added dropwise thionyl chloride (10.9 ml) under ice-cooling. The mixture is allowed to stand at room temperature overnight, and then evaporated to remove the solvent. To the residue is added isopropyl ether, and the mixture is washed, dried, and evaporated to remove the solvent. The resulting residue is distilled under reduced pressure to give (E)-3-methoxycarbonyl-4-phenyl-3-butenoic acid methyl ester (23.2 g) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514815 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-f8e6a35fff1d49518348a43bb22f4e2c |
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| Source note | uspto-grants-1996_05 |
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