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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948337Generated: October 30, 2026

Diethyl Oxalate → ethyl acetoacetate, sodium salt

https://huagongshe.com/reaction/1948337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Productethyl acetoacetate, sodium saltHCID 8519586%

Reaction Steps

Diethyl oxalate (10 g; 68 mmol) was dissolved in Et2O (100 ml) and cooled to −78 C. Ethyl magnesium bromide (1.0 M in THF; 72 ml; 71.8 mmol; 1.05 equiv.) was added slowly via syringe. The dry ice/acetone bath was allowed to melt and warm to 10 C. Monitored the reaction by 1H NMR. The reaction was cooled to 0 C and quenched with saturated NH4Cl. Dilute with H2O and separate phases. The organic layer was dried over Na2SO4, filtered and concentrated. Isolation gave 7.6 g of a crude yellow oil in 86% yield. No further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399489B2
Source datasetuspto-grants-2013_03
ORD IDord-22cf3ba8356c45edb857eab1138ed47f
Source noteuspto-grants-2013_03