HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858332Generated: October 30, 2026
Sodium Carbonate → HCID 23220910, compound
https://huagongshe.com/reaction/858332
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | 4-Carboxyphenylboronic Acid | HCID 312183 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 23220910 | HCID 23220910 | — |
Reaction Steps
In an 100 mL three-necked RB flask equipped with a magnetic bar, a condenser and a nitrogen gas inlet, 2-bromo-6-methoxynaphthalene (4.74 g, 20 mmol), 4-carboxybenzene boronic acid (3.50 g, 20 mmol) and 1-propanol (40 mL) were mixed and stirred at room temperature for approximately 30 min. Palladium acetate (0.014 g, 0.003 equiv., 0.06 mmol), triphenylphosphine (0.047 g, 0.009 equiv., 0.18 mmol), Na2CO3 solution (2M, 12 mL, 1.20 equiv., 24 mmol) and water (8 mL) were added and the mixture was refluxed for 1.5 h. When the mixture was still hot, 25 mL of water was added and the mixture was stirred and cooled to room temperature. The resultant crystals were filtered, washed with water and refluxed with 50 mL of acetic acid for 3–4 h. A white solid was obtained (5.08 g) and recrystallization from acetone showed the title compound as white crystals (4.63 g, 83%). mp 288–289° C. 1H NMR (500 MHz, DMSO) δ 3.90 (s, 3H), 7.2–8.3 (m, 10H), 12.99 (s, 1H). IR (KBr) ν (cm−1): 2500–3000 (COO—H, very broad, m), 1030 (OCH3, s), 1678 (C═O, s). Anal. Calcd for C18H14O3: C, 77.68; H, 5.07. Found: C, 77.56; H, 5.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07148311B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-088f35115aa04f36b21c3ba9ea9fdd54 |
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| Source note | uspto-grants-2006_12 |
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