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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385522Generated: October 31, 2026

Sulfuric Acid → Ethyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylate

https://huagongshe.com/reaction/385522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant5,6,7,8-TetrahydroquinoxalineHCID 36822—
ReactantSodium PersulfateHCID 62655—
ReactantSodium BicarbonateHCID 516892—
ReactantEthanedioic acid, monoethyl esterHCID 21943339—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductEthyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylateHCID 5781521622.1%

Reaction Steps

To a solution of 1.0 g of monoethyl oxalate in 14 mL of dichloromethane, 0.47 g of 5,6,7,8-tetrahydroquinoxaline, 91 μL of concentrated sulfuric acid, 1.7 g of sodium persulfate, and a suspension of 60 mg of silver nitrate in 14 mL of water were added, and the mixture was heated under reflux while stirring for 1 hour 30 minutes. To the reaction mixture, 1.7 g of sodium persulfate and 60 mg of silver nitrate were further added, and the mixture was heated under reflux for 1 hour 50 minutes. The reaction mixture was charged with chloroform and adjusted to pH 7.5 with a saturated aqueous sodium hydrogen carbonate solution, the insoluble substance was filtered off, and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by flash silica gel column chromatography using gradient elution with hexane:ethyl acetate=90:10 to 67:33 to obtain 0.16 g of ethyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylate as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-e1a8ee3a9e094d2c8fa46585a9fb96d4
Source noteuspto-grants-2013_02