Water → 2-Bromo-5-methoxybenzoic acid
Reaction equation
[C:1]([OH:11])(=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH3:9])[CH:3]=1.[Br:12]Br.O>C(O)(=O)C>[Br:12][C:7]1[CH:6]=[CH:5][C:4]([O:8][CH3:9])=[CH:3][C:2]=1[C:1]([OH:11])=[O:10]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To m-anisic acid in acetic acid (1 L) was added dropwise bromine (85 ml), followed by water (1 L). The reaction mixture was heated to reflux, cooled in an ice-bath and then the product was collected by filtration, washed with cold water and dried to afford 2-bromo-5-methoxybenzoic acid, m.p. 154°-156° C.
Workup
- temperatureThe reaction mixture was heated
- temperatureto reflux
- temperaturecooled in an ice-bath
- filtrationthe product was collected by filtration
- washwashed with cold water
- customdried
Sources & evidence
- ORD record
- ord-659aa404872c4533990d9c29e6ae22f1
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05488055
Reaction notes
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