HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25100Erstellt: 25. Oktober 2026
Iodide Ion → 5-(4-Methoxyphenyl)pent-4-yn-1-ol
https://huagongshe.com/reaction/25100
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Iodide Ion | HCID 30165 | — |
| Edukt | 4-Iodoanisole | HCID 69676 | — |
| Edukt | 4-Pentyn-1-ol | HCID 79346 | — |
| Katalysator | Triphenylphosphine | HCID 11776 | — |
| Katalysator | Palladium Chloride | HCID 24290 | — |
| Lösungsmittel | Diethylamine | HCID 8021 | — |
| Produkt | 5-(4-Methoxyphenyl)pent-4-yn-1-ol | HCID 11550138 | 88,9% |
Reaktionsschritte
4-Iodoanisol (10 g, 42 mmol), palladium (II) chloride (0.2 g, 1.1 mmol) and triphenylphosphine (0.6 g, 2.2 mmol) were dissolved in diethylamine (100 mL) then cupper(I) iodide (0.5 g, 2.2 mmol) and 4-pentyn-1-ol (5 mL, 53 mmol) were added. The reaction mixture was stirred overnight at room temperature, then the solvent was removed under reduced pressure. Ethyl acetate (150 mL) was added to the residue and the mixture was washed with 2N HCl, brine and water. The organic fraction was isolated, dried with sodium sulfate and the solvent was removed under reduced pressure. The product 16 (7.1 g. 87%) was isolated by flash chromatography (silica gel, 1:2 ethyl acetate/hexanes) as an oily yellow solid. 1H NMR (300 MHz, CDCl3) δ1.88 (m, 2H), 2.53 (m, 2H), 3.72 (s, 3H), 3.74 (m, 2H), 6.83 (d, 2H), 7.45 (d, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06858614B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-25ced7eb4bce4b60b9dcf3c7dc51c11f |
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| Quellennotiz | uspto-grants-2005_02 |
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