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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693368Generated: October 27, 2026

Diethyl Oxalate → Ethyl 3-(3-nitropyridin-2-yl)-2-oxopropionate

https://huagongshe.com/reaction/1693368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
Reactant2-Methyl-3-nitropyridineHCID 329360—
ReactantPotassium ethoxideHCID 23670592—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(3-nitropyridin-2-yl)-2-oxopropionateHCID 59753617—

Reaction Steps

To a solution of potassium ethoxide (2.44 g, 27.7 mmol) in diethyl ether (90 mL) and ethanol (8 mL) was added diethyl oxalate (3.79 mL, 27.7 mmol) resulting in a yellow suspension. The reaction mixture was stirred for 5 min prior to the addition of 2-methyl-3-nitropyridine (Preparation 29, 3.40 g, 24.6 mmol) in one portion. The resulting red suspension was stirred at rt, under argon, for 20 h. The mixture was filtered, washed thoroughly with diethyl ether and dried. The red solid was dissolved in water and the mixture adjusted to pH 4 by addition of glacial acetic acid. The resulting precipitate was collected by filtration, dissolved in dichloromethane, washed with brine, dried (MgSO4), and then filtered and concentrated in vacuo to give the title compound as an orange solid. δH (CDCl3): 1.40 (3H, t), 4.39 (2H, q), 7.34 (1H, s), 7.36 (1H, dd), 8.43 (1H, dd), 8.66 (1H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158622B2
Source datasetuspto-grants-2012_04
ORD IDord-348365cc819f496198e832965a856470
Source noteuspto-grants-2012_04