Reaction equation
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([Br:10])[C:7]([OH:11])=[C:6]([Br:12])[CH:5]=1.[CH3:14]I>>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:5]=[C:6]([Br:12])[C:7]([O:11][CH3:14])=[C:8]([Br:10])[CH:9]=1Participants
3
Procedure
3,5-Dibromo-4-methoxybenzoic acid methyl ester was prepared from 3,5-dibromo-4-hydroxybenzoic acid methyl ester by following Method C using methyl iodide as an alkylating agent in quantitative yield. The product was used without further purification.
Workup
- customThe product was used without further purification
Sources & evidence
- ORD record
- ord-834ee061903746239f419578b267c467
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691843B2
Linked notes
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