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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717282Generated: November 4, 2026

Ethyl Acetoacetate → HCID 68517178, compound

https://huagongshe.com/reaction/1717282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86629802HCID 86629802—
SolventEthanolHCID 702—
ProductHCID 68517178HCID 6851717828%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-azido-5-chloro-N-ethyl-2-methoxybenzamide (1.0 g) obtained in Example 73b) and ethyl 3-keto-n-butanoate (0.61 ml) in ethanol (20 ml) was added 20% sodium ethoxide in ethanol solution (1.85 ml) at room temperature, and the mixture was stirred at 60° C. for 5 hr. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a pale-brown solid (0.38 g, 28%). The obtained crude product was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803822B2
Source datasetuspto-grants-2010_09
ORD IDord-00d04b8c801a478396bb82a9f22ec9e9
Source noteuspto-grants-2010_09