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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44573Generated: October 26, 2026

Hydrochloric Acid → Ethyl (3-ethoxy-2-oxocyclohex-3-en-1-yl)(oxo)acetate

https://huagongshe.com/reaction/44573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant2-Ethoxycyclohex-2-en-1-oneHCID 121598—
ReactantHCID 178418261HCID 178418261—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (3-ethoxy-2-oxocyclohex-3-en-1-yl)(oxo)acetateHCID 4423543276%

Reaction Steps

41.40 g (0.29 mol) of 2-ethoxycyclohex-2-en-1-one were dissolved in 310 mL of diethyl ether and 325 mL of 1M LiN(TMS)2 in tetrahydrofuran were added dropwise at 50° C. After 30 minutes at the same temperature, 44.2 mL of diethyloxalate were also added under stirring. The solution was kept at room temperature overnight (TLC chloroform). 300 mL of water were then added, the pH adjusted to 4-5 by adding 1N HCl and the resulting solution extracted with ethyl acetate. The organic layer was dried over Na2SO4 and evaporated to dryness. The crude was purified by chromatography on a silica gel column eluted by chloroform (76% yield as an oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541429B2
Source datasetuspto-grants-2013_09
ORD IDord-60daf26c88204986beac783c16ac945c
Source noteuspto-grants-2013_09