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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838954Generated: November 3, 2026

Dichloromethane → 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/1838954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantHCID 178438045HCID 178438045—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamideHCID 11218717—

Reaction Steps

A mixture of 3-ethyl-4-nitro-1H-pyrazole-5-carboxamide (2.5 kg, 13.6 Mol), sodium carbonate (1.8 Kg, 17.0 Mol) and 2-bromoethyl methyl ether (1.98 kg, 14.2 Mol) in THF (22.5 L) and water (2.5 L) was heated under reflux and stirred for 20 hours. The mixture was cooled to ambient temperature and CH2Cl2 (67.5 L) and water (22.5 L) were added. The resultant organic and aqueous layers were separated. The aqueous phase was extracted with CH2Cl2 (22.5 L) and the combined organic solution was distilled under atmospheric pressure and replaced with ethyl acetate (33 L) to a final volume of 17 L. The cooled mixture was granulated at ambient temperature for 2 hours, filtered and washed with ethyl acetate (2.5 L). This afforded 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide as a white crystalline solid, 2.10 kg, 57%. m.p.=140° C. Found: C, 44.46; H, 5.79; N, 23.01. C9H14N4O4 requires C, 44.63; H, 5.79; N, 23.14%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677335B1
Source datasetuspto-grants-2004_01
ORD IDord-238c5669c86844fcb66eb8a16a5411b5
Source noteuspto-grants-2004_01