Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862260Generated: November 1, 2026

Methyl Lactate → 2-{1-(Methoxycarbonyl)ethoxy}-3-nitropyridine

https://huagongshe.com/reaction/1862260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl LactateHCID 11040—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-nitropyridineHCID 79613—
Solvent1,4-DioxaneHCID 31275—
Product2-{1-(Methoxycarbonyl)ethoxy}-3-nitropyridineHCID 2193357173%

Reaction Steps

0.8 g of sodium hydride was added to a mixture of 3.17 g of 2-chloro-3-nitropyridine, 2.19 g of methyl lactate and 20 ml of 1,4-dioxane at 10° C. The mixture was stirred at room temperature for 1.5 hours, then, poured into ice water, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 3.3 g of 2-{1-(methoxycarbonyl)ethoxy}-3-nitropyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06537948B1
Source datasetuspto-grants-2003_03
ORD IDord-8c35a9af41644d81880d7f86246997aa
Source noteuspto-grants-2003_03