HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087580Generated: October 31, 2026
2-Nitroimidazole → 3-[2-(2-Nitro-1H-imidazol-1-yl)ethyl]-2-oxazolidinone
https://huagongshe.com/reaction/1087580
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitroimidazole | HCID 10701 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(2-Chloroethyl)-1,3-oxazolidin-2-one | HCID 75633 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[2-(2-Nitro-1H-imidazol-1-yl)ethyl]-2-oxazolidinone | HCID 14896626 | 35.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05036096 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-ded9f9e7feb240488328798d7ef8a85e |
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| Source note | uspto-grants-1991_07 |
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