HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359221Generated: November 1, 2026
Potassium Hydroxide → 2-{[1-Bromo-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}-3-phenylpropanoic acid
https://huagongshe.com/reaction/1359221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-{[1-bromo-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}-3-phenylpropanoate | HCID 12082838 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-{[1-Bromo-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}-3-phenylpropanoic acid | HCID 10303446 | — |
Reaction Steps
Following the procedure described in Step 4 of Example 6, ethyl 2-{[1-bromo-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}-3-phenylpropanoate (1.85 g, 3.09 mmol) was hydrolyzed with potassium hydroxide (0.523 g, 9.32 mmol) in THF (20 mL) and water (20 mL). Crystallization from methylene chloride/hexane and drying at 78° C for 12 hours yielded 2-{[1-bromo-6-(3-pentanoyl-1-benzofuran-2-yl)-2-naphthyl]oxy}-3-phenylpropanoic acid a bright yellow solid (1.35 g), mp 115-117° C. Mass spectrum (+ESI, [M+H]+) m/z 573; 1HNMR (500 MHz, DMSO-d6): δ13.2-13.5 (br s, 1H), 8.45 (d, 1H, J=1.5 Hz), 8.2 (d, 1H, J=8.9 Hz), 8.1 (d, 1H, J=9.2 Hz), 8.05 (dd, 1H, J=7.7 Hz and 0.7 Hz), 8.0 (dd, 1H, J=8.9 Hz and 1.7 Hz), 7.75 (d, 1H, J=7.8 Hz), 7.4-7.45 (m, 6H), 7.3 (t, 2H, J=7.6 Hz), 7.25 (t, 1H, J=7.4 Hz), 5.35-5.4 (m, 1H), 2.75 (t, 2H, J=7.3 Hz), 1.5-1.6 (m, 2H), 1.1-1.2 (m, 2H), and 0.7 ppm (t, 3H, J=7.4 Hz). Elemental Analysis for C32H27BrO5.0.10H2O: Calculated: C, 67.05; H, 4.78; N, 0.00. Found: C, 66.69; H, 4.38; N, 0.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599925B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-d6b11a48f7c14a79b4f1d04c9d8ce147 |
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| Source note | uspto-grants-2003_07 |
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