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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031548Generated: October 31, 2026

2-Nitroimidazole → 3-[2-(2-Nitro-1H-imidazol-1-yl)ethyl]-2-oxazolidinone

https://huagongshe.com/reaction/1031548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitroimidazoleHCID 10701—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(2-Chloroethyl)-1,3-oxazolidin-2-oneHCID 75633—
SolventDimethylformamideHCID 6228—
Product3-[2-(2-Nitro-1H-imidazol-1-yl)ethyl]-2-oxazolidinoneHCID 1489662635.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 5 g (44 mmol) of 2-nitroimidazole and 6.1 g of K2CO3 in 50 ml of DMF was heated at 60° C. for 0.5 hours; then 6.61 g (44 mmol) of 3-(2-chloroethyl)-2-oxazolidinone was added and stirring continued for 18 hours; at 60° C. The mixture was then cooled and concentrated. The residue was partitioned between CHCl3 and water, the organic layer was dried and concentrated to a solid. The solid was crystallized from ethanol to give 3.5 g (35%) of the desired product, 3-[2-(2-nitro-1H-imidazol-1-yl)ethyl]-2-oxazolidinone; mp 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954515
Source datasetuspto-grants-1990_09
ORD IDord-37d2bd05c09c488b95565a6bd675550c
Source noteuspto-grants-1990_09