Sodium Hydroxide → HCID 86637918, compound
Reaction equation
[C:1]([N:9]([CH2:24][CH2:25][CH:26]([C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH2:10][CH2:11][CH2:12][C:13]1[CH:14]=[C:15]([CH:21]=[CH:22][CH:23]=1)[O:16][CH2:17][C:18]([OH:20])=[O:19])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+:40]>CO>[C:1]([N:9]([CH2:24][CH2:25][CH:26]([C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)[CH2:10][CH2:11][CH2:12][C:13]1[CH:14]=[C:15]([CH:21]=[CH:22][CH:23]=1)[O:16][CH2:17][C:18]([O-:20])=[O:19])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1.[Na+:40]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (3-{3-[benzoyl(3,3-diphenylpropyl)amino]propyl}phenoxy)acetic acid (110 mg) in MeOH (1 mL) was added 1M NaOH aqueous solution (0.217 mL) at ambient temperature. The mixture was stirred for 0.5 hours at the same temperature. The resulting mixture was evaporated in vacuo. The residue was triturated with diisopropylether to give a sodium (3-{3-[benzoyl(3,3-diphenylpropyl)amino]propyl}phenoxy)acetate.
Workup
- customThe resulting mixture was evaporated in vacuo
- customThe residue was triturated with diisopropylether
Sources & evidence
- ORD record
- ord-f475f0730ffc49a5b358b2138f5527a9
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08273745B2
Reaction notes
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