Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 4-Iodophenylacetate | HCID 141793 | — |
| Edukt | 1-Ethynyl-4-pentylbenzene | HCID 2775131 | — |
| Katalysator | Copper iodide | HCID 83717 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Diisopropylamine | HCID 7912 | — |
| Produkt | 4-[(4-Pentylphenyl)ethynyl]phenol | HCID 18671138 | — |
Reaktionsschritte
4-Pentylphenylacetylene (10.5 g, 61.4 mmol), 4-acetoxyphenyl iodide (16.1 g, 61.4 mmol), a catalytic amount of Pd(PPh3)2Cl2 and a catalytic amount of copper iodide were stirred in diisopropylamine (100 ml) at 70° C. After 5 minutes, a precipitate was seen and the mixture became unstirrable, toluene (100 ml) was added. The mixture was stirred at room temperature for 24 hours and then evaporated to dryness on a rotary evaporator. The residue was redissolved in aqueous potassium hydroxide ethanolic solution and stirred at 70° C. overnight. The mixture was evaporated to dryness, then partitioned between ethyl acetate and water, the organic phase was removed, dried and evaporated. The residue was purified by flash column chromatography using DCM as eluant. A pink coloured solid was left after evaporation of the appropriate fractions. Yield=10.4 g, 64%. 1H-NMR and IR spectroscopy gave the expected signals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06514578B1 |
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| Quelldatensatz | uspto-grants-2003_02 |
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| ORD ID | ord-fbc96aea378f44dca8347db3b9ca696d |
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| Quellennotiz | uspto-grants-2003_02 |
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