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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750398Generated: November 1, 2026

Ethyl 4-chloroacetoacetate → HCID 86721242, compound

https://huagongshe.com/reaction/1750398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-chloroacetoacetateHCID 69484—
ReactantHCID 86721241HCID 86721241—
SolventEthanolHCID 702—
ProductHCID 86721242HCID 8672124264.1%

Reaction Steps

A solution of the compound (2.80 g, 10.68 mmol) obtained in step 5 and ethyl 4-chloroacetoacetate (1.588 mL, 11.75 mmol) in ethanol (30 mL) was stirred at 80° C. for 16 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by NH-silica gel column chromatography (solvent gradient; 3→50% ethyl acetate/hexane) to give ethyl 2-(2-(5-bromo-1-tert-butyl-1H-pyrazol-4-yl)thiazol-4-yl)acetate (2.55 g, 6.85 mmol, 64%) as a colorless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-5a88134361ac4aa2b5655379b9aa6102
Source noteuspto-grants-2015_10