HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031549Generated: October 30, 2026
2-Nitroimidazole → 3-[3-(2-Nitro-1H-imidazol-1-yl)propyl]-2-oxazolidinone
https://huagongshe.com/reaction/1031549
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Nitroimidazole | HCID 10701 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(3-Chloropropyl)-2-oxazolidinone | HCID 13354964 | — |
| Product | 3-[3-(2-Nitro-1H-imidazol-1-yl)propyl]-2-oxazolidinone | HCID 14896627 | 81.7% |
Reaction Steps
A mixture of 6 9 of 2-nitroimidazole (53 mmol) and 7.32 g of K2CO3 was heated at 60° C. for 0.5 hours. Then 8.6 g (53 mmol) of 3-(3-chloropropyl)-2-oxazolidinone (Ann. Pharm. Franc., 13, 565 (1955)) 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 give 10.4 g of a solid which was recrystallized from ethanol to provide 5.4 g (42%) of the desired product, 3-[3-(2-nitro-1H-imidazol-1-yl)propyl]-2-oxazolidinone; mp 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04954515 |
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| Source dataset | uspto-grants-1990_09 |
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| ORD ID | ord-46a76c961fe8485c96b6db25dcb27e8a |
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| Source note | uspto-grants-1990_09 |
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