Sodium Hydroxide → HCID 86669791, compound
Reaction equation
C[O:2][C:3](=[O:42])[CH:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]1([C:24](=[O:41])[N:25]([C:32]1[O:40][C:36]2=[CH:37][CH:38]=[CH:39][C:35]2=[CH:34][CH:33]=1)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([CH:18]=[CH:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[CH:14][CH:13]=1.[OH-].[Na+]>CCO.C1COCC1.O>[O:40]1[C:36]2=[CH:37][CH:38]=[CH:39][C:35]2=[CH:34][CH:33]=[C:32]1[N:25]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:24]([C:5]1([CH2:10][CH2:11][C:12]2[CH:13]=[CH:14][C:15]([CH:18]=[CH:19][C:20]([CH3:23])([CH3:21])[CH3:22])=[CH:16][CH:17]=2)[CH:6]=[CH:7][CH:8]=[CH:9][CH:4]1[C:3]([OH:42])=[O:2])=[O:41]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of (R)-4-[2-(4-Benzofuran-2-yl-phenylcarbamoyl)-2-[4-(3,3-dimethyl-but-1-enyl)-phenyl-ethyl]-benzoic acid methyl ester (0.29 g, 0.52 mmol) in EtOH/THF/H2O (4:2:1) (12 mL) at rt, was added aq. 40% NaOH (2.5 ml), The reaction mixture was stirred for overnight, After completion of the reaction, the solvent was removed under reduced pressure. The crude was taken to pH=2 with 4N HCl and the resulting mixture was extracted with ethyl acetate. The organic layer was dried over MgSO4 and concentrated, the resulting compound was dried under vacuum to afford 4-[2-(4-Benzofuran-2-yl-phenylcarbamoyl)-2-[4-(3,3-dimethyl-but-1-enyl)-phenyl-ethyl]-benzoic acid as a solid (0.27 g, 98%):
Workup
- customAfter completion of the reaction
- customthe solvent was removed under reduced pressure
- extractionthe resulting mixture was extracted with ethyl acetate
- dry with materialThe organic layer was dried over MgSO4
- concentrationconcentrated
- customthe resulting compound was dried under vacuum
Sources & evidence
- ORD record
- ord-7f9efe6be4bd46889d4d671e34c6bd60
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09169201B2
Reaction notes
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