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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455084Generated: October 30, 2026

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

https://huagongshe.com/reaction/1455084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroformHCID 6212—
ReactantDiethyl OxalateHCID 7268—
Reactant2-Ethoxycyclohex-2-en-1-oneHCID 121598—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
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(1MS)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 1 N 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 numberUS07482354B2
Source datasetuspto-grants-2009_01
ORD IDord-0827f59a73ab45eaa6c858d94cafd6e6
Source noteuspto-grants-2009_01