Sodium Hydroxide → HCID 86759783, compound
Reaction equation
[OH-].[Na+:2].[CH2:3]([C:10]1[CH:43]=[CH:42][C:13]([O:14][CH2:15][CH2:16][CH2:17][N:18]2[C:22]([CH3:23])=[CH:21][CH:20]=[C:19]2[C:24]2[CH:41]=[CH:40][C:27]([O:28][C@H:29]([CH2:33][C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[C:30]([OH:32])=[O:31])=[CH:26][CH:25]=2)=[CH:12][CH:11]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9]>C(O)C>[CH2:3]([C:10]1[CH:11]=[CH:12][C:13]([O:14][CH2:15][CH2:16][CH2:17][N:18]2[C:22]([CH3:23])=[CH:21][CH:20]=[C:19]2[C:24]2[CH:25]=[CH:26][C:27]([O:28][C@H:29]([CH2:33][C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[C:30]([O-:32])=[O:31])=[CH:40][CH:41]=2)=[CH:42][CH:43]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[Na+:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethanol (6 ml) and a solution of 1N sodium hydroxide in ethanol (0.536 ml) were added to (2R)-2-(4-{1-[3-(4-heptylphenoxy)propyl]-5-methyl-1H-pyrrol-2-yl}phenoxy)-3-phenylpropanoic acid (330 mg, 0.596 mmol) and the mixture was concentrated. To the residue was added diisopropylether to give the object compound as a solid. 212 mg (yield: 68.6%)
Workup
- concentrationthe mixture was concentrated
- additionTo the residue was added diisopropylether
Sources & evidence
- ORD record
- ord-2f4e4cefc0c74f6595b6f7971d148e93
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06911468B2
Reaction notes
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