HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723520Generated: October 31, 2026
Sodium hydride → 6-Ethoxycarbonylmethoxy-5-nitro-nicotinic acid methyl ester
https://huagongshe.com/reaction/723520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | Methyl 6-chloro-5-nitronicotinate | HCID 346961 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Ethoxycarbonylmethoxy-5-nitro-nicotinic acid methyl ester | HCID 57896733 | 68.2% |
Reaction Steps
A solution of ethyl glyoxalate (2.80 g) in dry dioxan (100 mL), cooled in ice, was treated with sodium hydride (60% dispersion in oil; 1.30 g) and the mixture was heated at 50° C. for 30 minutes and cooled in ice. A solution of 6-chloro-5-nitro-nicotinic acid methyl ester (5.25 g) [prepared as described by A. H. Berrie et al. J. Chem. Soc. 2590-2594 (1951)] in dioxan (40 mL) was added and the solution was stirred at 0° C. for 30 minutes and then at room temperature overnight. The reaction mixture was evaporated to dryness, sodium bicarbonate solution was added to pH 7, and the mixture extracted with chloroform, dried (anhydrous sodium sulfate) and evaporated to afford a semi-solid that was chromatographed on silica gel [dichloromethane-hexane (1:1) then dichloromethane] to afford the product (4.70 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141564B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-f403910b223c4abba388c95e102534bb |
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| Source note | uspto-grants-2006_11 |
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