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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074071Generated: October 30, 2026

Methyl iodide → Ethyl 1-methyl-4-nitroimidazole-2-carboxylate

https://huagongshe.com/reaction/2074071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclohexane ethylacetateHCID 21867204—
ReactantHCID 178470305HCID 178470305—
SolventAcetoneHCID 180—
ProductEthyl 1-methyl-4-nitroimidazole-2-carboxylateHCID 2758876—

Reaction Conditions

Temperature60 °C

Reaction Steps

6.80 g (36.7 mmol) of ethyl 4-nitro-1H-imidazole-2-carboxylate are dissolved in 140 ml of acetone, and 11.2 g (80.8 mmol) of potassium carbonate and 4.57 ml (73.5 mmol) of iodomethane are added. The mixture is then stirred at 60° C. for 4 h. According to TLC (cyclohexane/ethyl acetate 2:1), the starting material has been converted completely. After cooling, the mixture is filtered, the residue is washed with dichloromethane and the filtrate is freed from the solvent. The solid obtained is dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919489B2
Source datasetuspto-grants-2011_04
ORD IDord-b793f13c47284608a67f50fde8aaafc1
Source noteuspto-grants-2011_04