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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075970Generated: October 26, 2026

Diazomethane → Ethanone, 1-(1-methyl-2-nitro-1H-imidazol-5-yl)-

https://huagongshe.com/reaction/1075970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
Reactant1-Methyl-2-nitro-1H-imidazole-5-carboxaldehydeHCID 100390—
SolventDiethyl EtherHCID 3283—
ProductEthanone, 1-(1-methyl-2-nitro-1H-imidazol-5-yl)-HCID 21503737—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.70 g. of 1-methyl-2-nitro-5-imidazolecarboxaldehyde in 180 ml. of diethyl ether, a solution of 0.43 g. of diazomethane in 86 ml. of diethyl ether is added under cooling at about 0° C. After standing at room temperature for 7 days, the reaction mixture is filtered and then evaporated to dryness. The residue (0.60 g.), dissolved, in 6 ml. of chloroform, is chromatographed on 6 plates of silica gel, eluting with a 9:1 (v/v) chloroform:methanol mixture, and TLC spots are visualized under U.V. light. The silica gel, which corresponds to an Rf value from 0.64 up to 0.76 is collected and extracted with methanol. From this solution, after filtration and concentration, 0.065 g. of 5-acetyl-1-methyl-2-nitroimidazole is obtained, m.p. 81°-83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954789
Source datasetuspto-grants-1976_05
ORD IDord-a72756c870e04875932f2d468ce98da2
Source noteuspto-grants-1976_05