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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011980Generated: October 30, 2026

Ethyl Acetoacetate → HCID 86626592, compound

https://huagongshe.com/reaction/1011980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86626593HCID 86626593—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 86626592HCID 86626592—

Reaction Steps

A solution of sodium ethanolate 21% (in ethanol, 0.75 ml, 2 mmol) was added to ethyl acetoacetate (0.25 ml, 1.97 mmol) in 3 ml ethanol at 0° C. After 1 h at 0° C., a solution of (2Z or E)-1-[3-(trifluoromethyl)phenyl]-2-(2,2,2-trifluoro-1-{[(4-methylphenyl)sulfonyl]-oxy}ethylidene)hydrazine (254 mg, 0.60 mmol) in 5 ml ethanol was added. Stirring was continued for 18 h at room temperature and then the yellow solution was diluted with EtOAc washed with water and brine. The combined organic layers were dried over magnesium sulfate and evaporated. Column chromatography (EtOAc:n-heptane 1:3) delivered the title compound as light yellow solid (107 mg, 48%). MS: 367.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977358B2
Source datasetuspto-grants-2011_07
ORD IDord-4be757c3bfbc4fddb7b3bf1113eb4ae8
Source noteuspto-grants-2011_07