Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917263Generated: October 26, 2026

Ethyl cyanoformate → Ethyl 4-ethoxy-2-oxocyclohex-3-ene-1-carboxylate

https://huagongshe.com/reaction/1917263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoformateHCID 69336—
Reactant3-Ethoxycyclohex-2-ene-1-oneHCID 79216—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-ethoxy-2-oxocyclohex-3-ene-1-carboxylateHCID 58997709—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of LDA (192 mmol) in THF (200 mL) was added 3-ethoxy-cyclohex-2-enone (23 mL) dropwise. After stirring for 1 h at −78° C., ethyl cyanoformate (16 mL) was added. The mixture was stirred at −78° C. for 4 h and then was warmed to rt and stirred for 1 h. The mixture was concentrated, diluted with aq. NH4Cl (300 mL), and poured into water. The resulting solids were collected by suction filtration and washed with hexanes followed by water, then was dried and concentrated to provide 17.1 g of a brown solid. TLC (SiO2, 33% EtOAc/hexanes): Rf=0.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618288B2
Source datasetuspto-grants-2013_12
ORD IDord-bbcc19a53b1445139b5e11a48fa3fafd
Source noteuspto-grants-2013_12