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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751628Generated: October 25, 2026

Diethyl Oxalate → Ethyl 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropanoate

https://huagongshe.com/reaction/751628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant6-Methoxy-2-methyl-3-nitropyridineHCID 230475—
ReactantPotassium ethoxideHCID 23670592—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropanoateHCID 59753655—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of potassium ethoxide (0.55 g, 6.55 mmol) in diethyl ether (20 mL, anhydrous) and ethanol (4 mL) was added diethyl oxalate (894 μL, 6.55 mmol) and the reaction mixture was stirred for 30 min prior to the addition of 6-methoxy-2-methyl-3-nitropyridine (Preparation 33, 1.0 g, 5.95 mmol) in diethyl ether (8 mL). The resulting red suspension was stirred at rt, under argon, for 20 h. The mixture was filtered, the solid washed thoroughly with diethyl ether then dried. The red solid was then taken up in hot water and the solution cooled to 0° C. The precipitate was filtered, washed with cold water, and dried to give the title compound as a beige solid. δH (CDCl3): 1.40 (3H, t), 4.07 (3H, s), 4.39 (2H, q), 6.74 (1H, d), 7.57 (1H, s), 8.40 (1H, d), 13.82 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405210B2
Source datasetuspto-grants-2008_07
ORD IDord-a4de3c39692d49fe8c4ff464c7f6d4d7
Source noteuspto-grants-2008_07