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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929754Generated: October 30, 2026

Ethanol → Ethyl 5-nitro-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/1929754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Nitro-1H-pyrazole-3-carboxylic acidHCID 86222684—
SolventWaterHCID 962—
ProductEthyl 5-nitro-1H-pyrazole-3-carboxylateHCID 8622290685%

Reaction Steps

To a solution of 5-nitropyrazol-3-carboxylic acid (19.9 g) in ethanol (200 mL) was added dropwise thionyl chloride (9.7 mL) over a period of 5 minutes and the mixture was refluxed for 4 hours. After cooling to room temperature, the reaction mixture was diluted with water (25 mL) and ethanol (50 mL) and to the mixture was neutralized with sodium hydrogencarbonate (54 g). The mixture was filtered and the residue was washed with ethanol. The filtrate and the washings were combined and concentrated in vacuo. The residue was azeotropically distilled with ethanol and the residue was dissolved in ethyl acetate, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and to the residue was added isopropylether. The precipitates were collected by filtration and washed with ethyl acetate/diisopropylether (1/2) to give ethyl 5-nitropyrazol-3-carboxylate (20 g, yield: 85%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188097B2
Source datasetuspto-grants-2012_05
ORD IDord-ef892678d68b465bbbee788d1f4593ec
Source noteuspto-grants-2012_05