Potassium Hydroxide → 2-{[6-(3-Pentanoyl-1-benzofuran-2-yl)-1-phenyl-2-naphthyl]oxy}acetic acid
Reaction equation
[C:1]([C:7]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[O:9][C:8]=1[C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][CH:25]=1)[C:22]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[C:21]([O:32][CH2:33][C:34]([O:36]CC)=[O:35])[CH:20]=[CH:19]2)(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[OH-].[K+]>C1COCC1.O>[C:1]([C:7]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[O:9][C:8]=1[C:16]1[CH:17]=[C:18]2[C:23](=[CH:24][CH:25]=1)[C:22]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[C:21]([O:32][CH2:33][C:34]([OH:36])=[O:35])[CH:20]=[CH:19]2)(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Following the procedure described in Step 4 of Example 6, ethyl 2-{[6-(3-pentanoyl-1-benzofuran-2-yl)-1-phenyl-2-naphthyl]oxy}acetate (0.161 g, 0.318 mmol) was hydrolyzed with potassium hydroxide (0.0693 g, 1.24 mmol) in THF (6 mL) and water (6 mL). 2-{[6-(3-pentanoyl-1-benzofuran-2-yl)-1-phenyl-2-naphthyl]oxy}acetic acid was obtained and was converted to the sodium salt by dissolving (0.103 g, 0.215 mmol) of the acid in methanol (5 mL) and adding 1N sodium hydroxide (0.22 mL, 22 mmol). After standing for 25 minutes, the mixture was solvent evaporated and the residue was rinsed with hexane and dried for 24 hours at 100° C. to give a yellow solid (0.0913 g), mp 272-273° C. (dec.). Mass spectrum (−ESI, [M−H]−) m/z 477. 1HNMR (500 MHz, DMSO-d6): δ8.35 (d, 1H, J=1.7 Hz), 8.05 (t, 2H, J=7.6 Hz), 7.65-7.7 (m, 2H), 7.5-7.55 (m, 3H), 7.35-7.45 (m, 6H), 4.25 (s, 2H), 2.75 (t, 2H, J=7.3 Hz), 1.5-1.55 (m, 2H), 1.1-1.2 (m, 2H), and 0.7 ppm (t, 3H, J=7.4 Hz). Elemental Analysis for C31H26O5Na.0.6H2O: Calculated: C, 72.82; H, 5.16; N, 0.00. Found: C, 72.57; H, 4.92; N, 0.05.
Sources & evidence
- ORD record
- ord-836a5f98f9a44f93b795a97f4e4fd65a
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06599925B2
Reaction notes
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