HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264599Erstellt: 25. Oktober 2026
Hydrochloric Acid → 4-(n-Pentoxyphenyl)-4'-carboxybiphenyl
https://huagongshe.com/reaction/264599
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 4-Iodobenzoic acid | HCID 12085 | — |
| Edukt | 4'-Pentyloxybiphenyl-4-boronic Acid | HCID 11358071 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4-(n-Pentoxyphenyl)-4'-carboxybiphenyl | HCID 21479550 | 70,9% |
Reaktionsschritte
To a stirred mixture of 4-(4-n-pentoxyphenyl)phenylboronic acid (1.0 g, 3.52 mmol) and 4-iodobenzoic acid (874 mg, 3.52 mmol) in ethanol (11 ml) and toluene (30 ml) was added an aqueous solution of sodium carbonate (2M, 5.3 ml, 10.6 mmol) followed by tetrakis(triphenylphosphine)palladium (204 mg, 5 mol %). The reaction mixture was heated at 100° C. under a nitrogen atmosphere for a period of 18 h. The cooled mixture was acidified to pH 3 (1N HCl) and partitioned between ethyl acetate and water. The organic phase was washed with water (3×) and brine, dried with magnesium sulfate, and filtered through a bed of Celite. The solvent was removed in vacuo to give crude product which was purified by flash silica gel chromatography to provide 4-(n-pentoxyphenyl)-4'-carboxybiphenyl (450 mg): 1H NMR (400 MHz, DMSO-d6) δ0.89 (t, 3H), 1.37 (m, 4H), 1.72 (m, 2H), 3.98 (t, 2H), 7.01 (d, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05646245 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-0ab78d509caa495cabb27b4ae2337c97 |
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| Quellennotiz | uspto-grants-1997_07 |
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