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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750426Generated: November 1, 2026

Ethyl 4-chloroacetoacetate → HCID 86721268, compound

https://huagongshe.com/reaction/1750426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
ReactantHCID 86721266HCID 86721266—
SolventEthanolHCID 702—
ProductHCID 86721268HCID 8672126869%

Reaction Steps

A solution of the mixture (415 mg, 1.29 mmol) obtained in step 6 and ethyl 4-chloroacetoacetate (0.192 mL, 1.42 mmol) in EtOH (3.6 mL) was heated under reflux for 4 hr. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The solution was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine and dried, and the solvent was evaporated under reduced pressure. The residue was purified by NH-silica gel column chromatography (solvent gradient; 50→66% ethyl acetate/hexane) to give ethyl {2-[5-(4-fluorophenyl)-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate (294 mg, 69%) was obtained as a colorless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-931aa05bca1949b591631809bca9ab1b
Source noteuspto-grants-2015_10