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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642769Generated: November 2, 2026

Acetic Acid → 1,4-Dinitro-1H-imidazole

https://huagongshe.com/reaction/1642769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitric AcidHCID 944—
ReactantHCID 178526856HCID 178526856—
SolventWaterHCID 962—
Product1,4-Dinitro-1H-imidazoleHCID 5169496—

Reaction Steps

430 mL of acetic acid and 188 g of 4-nitroimidazole were charged into a 2 L-volume reactor and stirred. While stirring the mixture, 100% nitric acid(137 mL) was slowly added dropwise to the mixture at the reaction temperature of 35° C. Anhydrous acetic acid(318 mL) was added dropwise thereto at 25° C. over 1 hour. After stirring the reaction mixture at 25° C. for 2 days, 1,4-dinitroimidazole was synthesized. Then, the resultant was poured in 2 L cold water, and extracted three times with 500 mL of methyl chloride for each time. The obtained methylene chloride solution was dried over MgSO4 so as to completely remove the water therefrom, resulting in methylene chloride extract solution containing 1,4-dinitroimidazole. The structure of the obtained 1,4-dinitroimidazole was as same as that of the comparative example.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119679B2
Source datasetuspto-grants-2012_02
ORD IDord-237c03f6665b44e9b6d3d3986fb5e074
Source noteuspto-grants-2012_02