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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-methyl-5-nitro-2(1H)-pyridinoneHCID 295866—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Bromo-1-methyl-5-nitro-2(1H)-pyridinoneHCID 6726748172.15%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-57a353319efd4a0f9f44814c4bb2984f
Source noteuspto-grants-2011_03