HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1181Erstellt: 23. Oktober 2026
Water → 4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenyl
https://huagongshe.com/de/reaction/1181
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Bromo-1,2-difluorobenzene | HCID 67675 | — |
| Edukt | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Edukt | 4-(4-Propylcyclohexyl)-phenyltrimethoxysilane | HCID 10860253 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenyl | HCID 612306 | 94,5% |
Reaktionsschritte
To 0.645 g (2 mmol) of 4-(4-propylcyclohexyl)-phenyltrimethoxysilane (Ih) was added 2.1 ml of TBAF (2.1 mmol, 1M in THF) under nitrogen, and the mixture was stirred at room temperature for 30 minutes. After the solvent was removed under reduced pressure, a solution of 3,4-difluorobromobenzene (0.463 g, 2.4 mmol) in toluene (1 ml) was added, followed by the addition of a suspension of tetrakis(triphenylphosphine)palladium(0) (0.116 g, 0.1 mmol) in toluene (3 ml). The resulting mixture was refluxed for 3 hours. After cooling, to the reaction mixture were added water and toluene. The organic layer was separated and the aqueous layer was extracted with toluene three times. The combined organic layer was dried over magnesium sulfate. After the magnesium sulfate was removed by filtration, the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (heptane) to obtain 0.594 g (40%) of white crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05723621 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-f5c19c1716b641f7a3721e4238a2fc65 |
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| Quellennotiz | uspto-grants-1998_03 |
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