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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092891Generated: November 1, 2026

Dimethylformamide → (R)-1-(2-methyl-2-oxiranylmethyl)-4-nitro-2-(4-nitrobenzenesulfonyl)imidazole

https://huagongshe.com/reaction/1092891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantCesium fluorideHCID 25953—
ReactantHCID 178526725HCID 178526725—
SolventWaterHCID 962—
Product(R)-1-(2-methyl-2-oxiranylmethyl)-4-nitro-2-(4-nitrobenzenesulfonyl)imidazoleHCID 8660437631%

Reaction Steps

4-Nitro-2-(4-nitrobenzenesulfonyl)imidazole (200 mg) and N,N-dimethylformamide (0.57 ml) suspension of 2-methyl-2-oxiranylmethyl(S)-4-nitrobenzenesulfonate (183 mg), potassium carbonate (120 mg) and cesium fluoride (20 mg) were stirred at a room temperature for 1.5 days. Water and ethyl acetate were added to the reaction mixture, and organic layer was taken by separation. The ethyl acetate layer was washed with water and an aqueous solution being saturated with sodium chloride, then dried over anhydrous sodium sulfate. The residue obtained by removal of the solvent by distillation was purified by use of a silica gel column chromatography (eluent: n-hexane/ethyl acetate=11/9 to 1/1), there was obtained (R)-1-(2-methyl-2-oxiranylmethyl)-4-nitro-2-(4-nitrobenzenesulfonyl)imidazole (76 mg, yield: 31%) as white powdery product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129544B2
Source datasetuspto-grants-2012_03
ORD IDord-e657a733acc447ef8d5ef8f7997712f5
Source noteuspto-grants-2012_03