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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107146Generated: October 31, 2026

Ethyl Acetoacetate → HCID 23047731, compound

https://huagongshe.com/reaction/2107146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 10753909HCID 10753909—
SolventEthanolHCID 702—
ProductHCID 23047731HCID 23047731—

Reaction Steps

A solution of 6.0 g (46 mmol) of ethyl acetoacetate in 6 ml of absolute ethanol is added drop by drop, with stirring, to a solution of 23 mmol of sodium ethylate in 18 ml of ethanol. Stirring is continued for another 15 minutes to complete the salt formation, and then a solution of 6.0 g (23 mmol) of 5-(4-chlorophenyl)pentyl bromide in 6 ml of absolute ethanol is added. The mixture is then heated for 3 hours with refluxing, and then completely concentrated by evaporation. Water is added to the concentrate and the mixture is neutralized with 2N hydrochloric acid. Then the organic components are extracted with ether, the combined extracts are dried, and are concentrated by evaporation. The concentrate is chromatographed on silica gel with a mixture of n-heptane and butanone. Yield: 5.8 g (81% of theory) of ethyl 2-acetyl-7-(4-chlorophenyl)heptanoate, a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933367
Source datasetuspto-grants-1990_06
ORD IDord-8c33e973386c4c259a9a9d8849ed8177
Source noteuspto-grants-1990_06