HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554879Erstellt: 25. Oktober 2026
1-Ethynyl-4-pentylbenzene → 2,5-Dibromo-3-(4-pentylphenyl)ethynylthiophene
https://huagongshe.com/reaction/554879
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Ethynyl-4-pentylbenzene | HCID 2775131 | — |
| Edukt | 2,5-Dibromo-3-iodothiophene | HCID 13011178 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 2,5-Dibromo-3-(4-pentylphenyl)ethynylthiophene | HCID 67461393 | — |
Reaktionsschritte
To a solution of 2,5-dibromo-3-iodothiophene (3.52 grams, 9.57 mmol) and 1-ethynyl-4-pentylbenzene (1.65 grams, 9.57 mmol) in triethylamine (50 milliliters) were added dichlorobis(triphenylphosphine)palladium (II) (0.28 gram, 0.4 mmol) and copper(I) iodide (38 milligrams, 0.2 mmol) at 0° C. under argon. The resulting reaction mixture was stirred at 0° C. for 6 hours and at room temperature for 20 hours under argon. After evaporation of the solvent, the product obtained was purified by column chromatography on a silica gel using hexane as eluent. 2,5-Dibromo-3-(4-pentylphenyl)ethynylthiophene was obtained as a colorless liquid was. Yield: 3 grams (73 percent).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08049205B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-b02a38216ee44f9e9bba10618600342b |
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| Quellennotiz | uspto-grants-2011_11 |
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