Nitric Acid → 2-Bromo-1,3-dimethyl-4-nitrobenzene
Reaction equation
[N+:1]([O-:4])(O)=[O:2].[CH3:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[C:7]=1[Br:13]>>[CH3:5][C:6]1[C:11]([N+:1]([O-:4])=[O:2])=[CH:10][CH:9]=[C:8]([CH3:12])[C:7]=1[Br:13]Participants
3
Conditions
- Temperature
- 80 °C
Procedure
Fuming nitric acid (83.3 mL) (>90%) was added slowly to a solution of 2,6-dimethyl bromobenzene (27.9 g, 150 mmol) in acetric acid (167 mL) and cooled in an ice-bath (above f.p). The mix was allowed to come to rt and later heated at 80° C. for 2 h. (HPLC showed no SM). Reaction mixture was cooled and poured into ice-water with stirring. The resulting yellow solid was filtered, washed with ice-water and dried to give 28.7 g of an yellow solid which was used as such in the next step.
Workup
- temperaturecooled in an ice-bath (above f.p)
- customto come to rt
- customReaction mixture
- temperaturewas cooled
- filtrationThe resulting yellow solid was filtered
- washwashed with ice-water
- customdried
Sources & evidence
- ORD record
- ord-8d8961b4498f45c493c8ac48ba937f36
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08071609B2
Reaction notes
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