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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 2-Methyl-3-nitropyridine | HCID 329360 | — |
| Reactant | Potassium ethoxide | HCID 23670592 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 3-(3-nitropyridin-2-yl)-2-oxopropionate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158622B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-348365cc819f496198e832965a856470 |
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| Source note | uspto-grants-2012_04 |
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