Hydrochloric Acid → HCID 86608475, compound
Reaction equation
[Cl:1][C:2]1[C:11]([NH:12][S:13]([C:16]([F:19])([F:18])[F:17])(=[O:15])=[O:14])=[CH:10][C:9]([Cl:20])=[CH:8][C:3]=1[C:4]([O:6]C)=[O:5].[OH-].[Na+].Cl>CO>[ClH:1].[Cl:1][C:2]1[C:11]([NH:12][S:13]([C:16]([F:19])([F:17])[F:18])(=[O:14])=[O:15])=[CH:10][C:9]([Cl:20])=[CH:8][C:3]=1[C:4]([OH:6])=[O:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Crude methyl 2,5-dichloro-3-{[(trifluoromethyl) sulfonyl]amino}benzoate (4.0 g) was dissolved in methanol (30 ml) and 4N NaOH (30 ml) was added while stirring at room temperature for 18 hrs. Removed solvent and added 4N HCl (10 ml). Stirred at room temperature for 4 hours. Filtered off solid to give 2,5-dichloro-3-{[(trifluoromethyl) sulfonyl]amino}benzoic acid hydrochloride in quantitative yield.
Workup
- stirringStirred at room temperature for 4 hours
- filtrationFiltered off solid
Sources & evidence
- ORD record
- ord-1760d859c53c490999605a2e2098870e
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07645771B2
Reaction notes
Loading…