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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067306Generated: October 31, 2026

Dimethyl Succinate → HCID 54348894, compound

https://huagongshe.com/reaction/1067306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SuccinateHCID 7820—
ReactantDiisopropyl EtherHCID 7914—
Reactant3,5-DimethoxybenzaldehydeHCID 81747—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54348894HCID 54348894124.5%

Reaction Steps

Potassium tert-butoxide (14.2 g) is dissolved in tert-butyl alcohol (120 ml), and thereto is added dropwise a solution of 3,5-dimethoxybenzaldehyde (20 g) and dimethyl succinate (21.1 g) in tetrahydrofuran. The mixture is stirred at room temperature for 30 minutes, and water and isopropyl ether are added to the mixture. The aqueous layer is separated, and the remaining organic layer is further extracted with water. The aqueous layers are combined, and the pH value thereof is adjusted to pH 2-3 with conc. hydrochloric acid. The resulting oily product is extracted with ethyl acetate, and the extract is dried, concentrated under reduced pressure to give 4-(3,5-dimethoxyphenyl)-3-carboxy-3-butenoic acid methyl ester (42 g) as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248743B1
Source datasetuspto-grants-2001_06
ORD IDord-b90867a062d4456380c582a12860ed41
Source noteuspto-grants-2001_06