Hydrochloric Acid → 2-Bromo-4-nitro-1H-imidazole
Reaction equation
[Br:1][C:2]1[N:3](COC)[CH:4]=[C:5]([N+:7]([O-:9])=[O:8])[N:6]=1.Cl>CO>[Br:1][C:2]1[NH:3][CH:4]=[C:5]([N+:7]([O-:9])=[O:8])[N:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Solution of 2-bromo-1-methoxymethyl-4-nitroimidazole (11.17 g), methanol (10 ml) and 5N hydrochloric acid (60 ml) was stirred under refluxing condition for 2.5 hours. After being let to stand the reaction mixture at a room temperature for 24 hours, the mixture was stirred for 1 hour under ice-cooling condition, the precipitated crystals were collected by filtration, and dried at 50° C. under a reduced pressure for 24 hours, there was obtained 2-bromo-4-nitroimidazole (6.0 g, yield: 66.0%) of white powdery product.
Workup
- temperatureunder refluxing condition for 2.5 hours
- customat a room temperature
- customfor 24 hours
- temperaturecooling condition
- filtrationthe precipitated crystals were collected by filtration
- customdried at 50° C. under a reduced pressure for 24 hours
Sources & evidence
- ORD record
- ord-cc471949238b4a308ac210e8c9dcbb5d
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129544B2
Reaction notes
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