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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281237Generated: October 28, 2026

Ethyl 4-chloroacetoacetate → HCID 12953391, compound

https://huagongshe.com/reaction/2281237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
Reactant4-FluorothiobenzamideHCID 737223—
SolventEthanolHCID 702—
ProductHCID 12953391HCID 12953391—

Reaction Steps

To a stirred solution of 4-fluorothiobenzamide (8.94 g, 57.6 mmol) in ethanol (70 mL) was added ethyl 4-chloroacetoacetate (7.8 mL, 58 mmol). The reaction was heated at reflux for 4 hours, treated with an addition aliquot of ethyl 4-chloroacetoacetate (1.0 mL, 7.4 mmol) and refluxed for an additional 3.5 hours. The reaction was then concentrated and the residue was partitioned between ethyl acetate (200 mL) and aqueous NaHCO3 (200 mL). The organic layer was combined with a backextract of the aqueous layer (ethyl acetate, 1×75 mL), dried (Na2SO4) and concentrated. The resulting amber oil was purified by flash chromatography using a hexane/ethyl acetate gradient to afford ethyl 2-(2-(4-fluorophenyl)thiazol-4-yl)acetate as a low melting, nearly colorless solid (13.58 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139580B2
Source datasetuspto-grants-2015_09
ORD IDord-7a713490660240e598306f00f22b9861
Source noteuspto-grants-2015_09