HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598052Generated: October 30, 2026
N-bromobutanimide → 3-Bromo-1-methyl-5-nitro-2(1H)-pyridinone
https://huagongshe.com/reaction/598052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-methyl-5-nitro-2(1H)-pyridinone | HCID 295866 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-1-methyl-5-nitro-2(1H)-pyridinone | HCID 67267481 | 72.15% |
Reaction Steps
To a solution containing 0.55 g (3.57 mmol) of 1-methyl-5-nitropyridin-2(1H)-one in 10 ml of N,N-dimethylformamide under a nitrogen atm. was added 0.76 g (4.27 mmol) of N-bromosuccinimide. The reaction was allowed to stir at 25° C. overnight. The reaction was diluted with dichloromethane and washed with water. The organic phase was dried over magnesium sulfate. Filtration, removal of solvent and purification of the residue via biotage eluting with 70% ethyl acetate/hexanes gave 0.60 g (72.15%) of product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897607B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-57a353319efd4a0f9f44814c4bb2984f |
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| Source note | uspto-grants-2011_03 |
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