HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873386Erstellt: 26. Oktober 2026
Water → 2-[4-(4-Propylcyclohexyl)phenyl]selenophene
https://huagongshe.com/reaction/1873386
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-Iodoselenophene | HCID 142183 | — |
| Edukt | 4-(trans-4-Propylcyclohexyl)phenylboronic Acid | HCID 3104710 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Toluene ethanol | HCID 21863594 | — |
| Produkt | 2-[4-(4-Propylcyclohexyl)phenyl]selenophene | HCID 59456296 | — |
Reaktionsschritte
A mixture 0111.0 g (41.1 mmol) of 2-iodoselenophene, 7.98 g (32.4 mmol) of 4-(4-propylcyclohexyl)phenylboronic acid, 3.70 g (3.20 mmol) of tetrakis(triphenylphosphine)palladium(0) and 60 ml of 2 N sodium carbonate soln. in 160 ml of toluene/ethanol (1:1) is heated under reflux for 22 h. After cooling, water is added, and the batch is extracted a number of times with MTBE. The combined organic phases are washed with water, sat. sodium hydrogencarbonate soln., 1 N hydrochloric acid and sat. sodium chloride soln. The solution is dried using sodium sulfate and concentrated to dryness. The residue is purified by column chromatography (SiO2, n-heptane:EtOAc=20:1). The further purification is carried out by recrystallisation from n-heptane; 2-[4-(4-propylcyclohexyl)phenyl]selenophene is obtained as a colourless solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08304036B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-76e1073097df4d6c889c3db6f8abdc88 |
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| Quellennotiz | uspto-grants-2012_11 |
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