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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl oxoacetateHCID 70211—
ReactantMethyl 6-chloro-5-nitronicotinateHCID 346961—
Solvent1,4-DioxaneHCID 31275—
Product6-Ethoxycarbonylmethoxy-5-nitro-nicotinic acid methyl esterHCID 5789673368.2%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141564B2
Source datasetuspto-grants-2006_11
ORD IDord-f403910b223c4abba388c95e102534bb
Source noteuspto-grants-2006_11