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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386738Generated: November 1, 2026

Nitric Acid → 6-Methoxycarbonylmethoxy-5-nitro-nicotinic acid ethyl ester

https://huagongshe.com/reaction/2386738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium hydrideHCID 24758—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantLactateHCID 91435—
ReactantEthyl 6-chloro-5-nitronicotinateHCID 3784053—
ReactantHCID 178418479HCID 178418479—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-Methoxycarbonylmethoxy-5-nitro-nicotinic acid ethyl esterHCID 67547085—

Reaction Steps

To a solution of 6-chloro-5-nitro-nicotinic acid ethyl ester (10.5 g, prepared from 6-hydroxy-nicotinic acid with a) fuming nitric acid, b) PCl5, POCl3, c) EtOH, see WO2005012288) in dioxan (100 ml) was added methylglycolate (4.92 g). Sodium hydride (55% dispersion in mineral oil, 2.19 g) was added portion wise at 0° C. The mixture was stirred at room temperature for 24 h. Water was added and the mixture was extracted with EtOAc. The organic phase was dried (MgSO4), filtered and concentrated to dryness. The product was purified by chromatography (SiO2, cyclohexane/EtOAc 1:0=>7:3) to give the title compound (3.026 g) as yellow oil. MS (m/e)=285.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268820B2
Source datasetuspto-grants-2012_09
ORD IDord-fc8596174a8146999afb95990bb53087
Source noteuspto-grants-2012_09