Sodium Hydroxide → HCID 69920491, compound
Reaction equation
[CH:1]([N:4]([S:28]([C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)(=[O:30])=[O:29])[C:5]1[CH:23]=[CH:22][C:21]([C:24]([F:27])([F:26])[F:25])=[CH:20][C:6]=1[O:7][CH2:8][C:9]1[CH:19]=[CH:18][C:12]([CH:13]=[CH:14][C:15]([OH:17])=[O:16])=[CH:11][CH:10]=1)([CH3:3])[CH3:2].[OH-].[Na+:38]>CO>[Na+:38].[CH:1]([N:4]([S:28]([C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1)(=[O:29])=[O:30])[C:5]1[CH:23]=[CH:22][C:21]([C:24]([F:26])([F:25])[F:27])=[CH:20][C:6]=1[O:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([CH:13]=[CH:14][C:15]([O-:17])=[O:16])=[CH:18][CH:19]=1)([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 4-[2-(N-isopropyl-phenylsulfonylamino)-5-trifluoromethylphenoxymethyl]cinnamic acid (425 mg; prepared in Example 18(40).) in MeOH (5 ml), 2N NaOH (0.41 ml) was added. The mixture was stirred at room temperature. The mixture was distilled off azeotropically with benzene three times to give the title compound (430 mg) having the following physical data.
Workup
- distillationThe mixture was distilled off azeotropically with benzene three times
Sources & evidence
- ORD record
- ord-79d65e22f02940b788fc3d43885b4faf
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06790866B2
Reaction notes
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