Ethyl 4-amino-3-bromo-5-chlorobenzoate → 4-Amino-3-bromo-5-chlorobenzoic acid
Reaction equation
[NH2:1][C:2]1[C:12]([Cl:13])=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][C:3]=1[Br:14]>Cl.CCO>[NH2:1][C:2]1[C:12]([Cl:13])=[CH:11][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[Br:14]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 21.0 g (75.4 mmol) ethyl 4-amino-3-bromo-5-chloro-benzoate in 200 mL 4 M HCl and 100 mL EtOH was refluxed overnight. After cooling the precipitate formed was suction filtered and dried.
Workup
- temperatureAfter cooling the precipitate
- customformed
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-c395370c4f31448db0ea7eb55f0855cb
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696209B2
Reaction notes
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