3-Hydroxybenzoic Acid → 4-Bromo-3-hydroxybenzoic acid
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[Br:11]Br>C(O)(=O)C>[Br:11][C:10]1[CH:9]=[CH:8][C:4]([C:5]([OH:7])=[O:6])=[CH:3][C:2]=1[OH:1]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In acetic acid (24.5 ml), 3-hydroxybenzoic acid (5.00 g) was suspended. To the resulting suspension, a solution of bromine (1.9 ml) in acetic acid (acetic acid: 5 ml) was added dropwise under ice cooling, followed by stirring at room temperature for 33 hours. The reaction mixture was ice cooled. The crystals so precipitated were collected by filtration and then washed with acetic acid, whereby the title compound (1.68 g, 21%) was obtained.
Workup
- temperaturecooled
- customThe crystals so precipitated
- filtrationwere collected by filtration
- washwashed with acetic acid, whereby the title compound (1.68 g, 21%)
- customwas obtained
Sources & evidence
- ORD record
- ord-7e05f6e5bc63485a8c1d080935a62e8b
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06747023B1
Reaction notes
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