Sodium Hydroxide → 3-Fluoro-6-(trifluoromethylsulfamoyl)-benzoic acid
Reaction equation
C[O:2][C:3](=[O:19])[C:4]1[C:9]([S:10](=[O:17])(=[O:16])[NH:11][C:12]([F:15])([F:14])[F:13])=[CH:8][CH:7]=[C:6]([F:18])[CH:5]=1.[OH-].[Na+]>O1CCOCC1>[F:18][C:6]1[CH:5]=[C:4]([C:9]([S:10](=[O:16])(=[O:17])[NH:11][C:12]([F:14])([F:15])[F:13])=[CH:8][CH:7]=1)[C:3]([OH:19])=[O:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Analogously to Example 21(b), 2.41 g (8 mmol) of 3-fluoro-6-(trifluoromethylsulfamoyl)-benzoic acid methyl ester in aqueous dioxane is saponified with NaOH and isolated. 1.55 g=67.3% of the theoretical yield is obtained as a partially crystalline product.
Workup
- customisolated
- custom1.55 g=67.3% of the theoretical yield
- customis obtained as a partially crystalline product
Sources & evidence
- ORD record
- ord-c1e3d1a889934aac9ddb837c969f0953
- Source dataset
- uspto-grants-1992_07
- Patent number
- US05130119
Reaction notes
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