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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34905Generated: October 27, 2026

Ethyl bromoacetate → HCID 13853976, compound

https://huagongshe.com/reaction/34905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant4-ThiazolidinoneHCID 637591—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13853976HCID 13853976—

Reaction Steps

A solution of 4-oxothiazolidine (50 g) in tetrahydrofuran (900 ml) was added dropwise to a suspension of sodium hydride (60% dispersion in mineral oil) (22.6 g) in tetrahydrofuran (850 ml) at room temperature and the mixture was allowed to warm up to reflux temperature. After the mixture was refluxed for an additional 30 minutes, ethyl bromoacetate (60 ml) was added dropwise under that condition. The mixture was refluxed further 1 hour and then cooled. Insoluble materials were removed by filtration. The filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography by eluting with chloroform to give ethyl 4-oxo-3-thiazolidinylacetate (78.5 g) as light brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764514
Source datasetuspto-grants-1988_08
ORD IDord-f55b41624f3049e8a1e0f3dc130644a9
Source noteuspto-grants-1988_08