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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDimethyl SuccinateHCID 7820—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product(E)-3-methoxycarbonyl-4-phenyl-3-butenoic acid methyl esterHCID 618659066.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514815
Source datasetuspto-grants-1996_05
ORD IDord-f8e6a35fff1d49518348a43bb22f4e2c
Source noteuspto-grants-1996_05