Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177329Generated: November 4, 2026

Diethyl Succinate → HCID 66756012, compound

https://huagongshe.com/reaction/1177329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl SuccinateHCID 31249—
Reactant5-Methyl-2-thiophenecarboxaldehydeHCID 61663—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 66756012HCID 6675601261%

Reaction Steps

Sodium ethylate (6.5 g, 95 mmol) was added under vigorous stirring to a solution of 5-methylthiophene-2-carbaldehyde (10 g, 79 mmol) and diethyl succinate (27.6 g, 158 mmol) in ethanol (300 mL). The reaction mixture was refluxed for 3 h and evaporated in vacuum (˜20 mmHg) at 50° C. until the solvent distillation ceased. The obtained residue was diluted with 200 mL of 10% HCl and 300 mL of ethyl acetate. The mixture was shaken. The organic layer was separated, diluted with 200 mL of a saturated aqueous solution of NaHCO3, and shaken. The aqueous layer was separated, neutralized by 10% HCl to pH 2, and subjected to extraction by 400 mL of ethyl acetate. The organic layer was evaporated in vacuum (˜20 mmHg) at 60° C. and chromatographed on a layer of silica gel (200×150 mm) with hexane/ethyl acetate mixture, 1:1 as eluent. Fractions containing the target product were collected and evaporated in vacuum to give 12.3 g (48 mmol, 61%) of 3-(ethoxycarbonyl)-4-(5-methyl-2-thienyl)but-3-enoic acid as a light-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-f1e07138f8c446adbba4e6c0f112f0cc
Source noteuspto-grants-2010_11