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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Bromo-1,2-difluorobenzeneHCID 67675—
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt4-(4-Propylcyclohexyl)-phenyltrimethoxysilaneHCID 10860253—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
Produkt4'-(trans-4-Propylcyclohexyl)-3,4-difluorobiphenylHCID 61230694,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723621
Quelldatensatzuspto-grants-1998_03
ORD IDord-f5c19c1716b641f7a3721e4238a2fc65
Quellennotizuspto-grants-1998_03