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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862331Generated: November 2, 2026

Tetrahydrofuran → Ethyl 2-(3-nitropyridin-2-yl)oxyacetate

https://huagongshe.com/reaction/1862331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl GlycolateHCID 12184—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-nitropyridineHCID 79613—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-nitropyridin-2-yl)oxyacetateHCID 442597585.4%

Reaction Steps

11 g of sodium hydride was added to a mixture of 39.63 g of 2-chloro-3-nitropyridine, 31.23 g of ethyl glycolate, 250 ml of tetrahydrofuran and 20 ml of N,N-dimethylformamide at 0° C. The mixture was stirred at room temperature for 5 hours, then, the reaction solution was 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 48.3 g of 2-(ethoxycarbonyl)methoxy-3-nitropyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06537948B1
Source datasetuspto-grants-2003_03
ORD IDord-a4af2e54ae83403fae16651a5115369e
Source noteuspto-grants-2003_03