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HRID 1847100Erstellt: 27. Oktober 2026

Potassium Carbonate → 2,3,4,5,5',6-Hexafluoro-2'-methoxy-1,1'-biphenyl

https://huagongshe.com/reaction/1847100

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPentafluoroiodobenzeneHCID 70008—
Edukt5-Fluoro-2-methoxyphenylboronic acidHCID 2782673—
KatalysatorTetrabutylammonium BromideHCID 74236—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
Produkt2,3,4,5,5',6-Hexafluoro-2'-methoxy-1,1'-biphenylHCID 86710453277,5%

Reaktionsschritte

Compound 1 (6.3 g, 3.7 mmol, 1 equiv) and iodopentafluorobenzene (5.5 mL, 4 mmol, 1.2 equiv) were dissolved in toluene (120 mL). 1.0 M Potassium carbonate solution (120 mL), tetrabutylammonium bromide (600 mg), and tetrakis(triphenylphosphine)palladium(0) (2.1 g, 1.8 mmol, 0.05 equiv) were added. Nitrogen was sparged through the mixture for 10 minutes. The reaction was refluxed 18 hours, then cooled to room temperature. The layers were separated and the aqueous layer was extracted with methyl tert-butyl ether (2×50 mL). The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified over silica gel (100 g), eluting with a gradient of 0 to 4% ethyl acetate in heptane to give 2,3,4,5,5′,6-hexafluoro-2′-methoxy-1,1′-biphenyl (2) (3.0 g, 28% yield) as an off-white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08952114B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-9428941c0fc94688951be6ebf416a85b
Quellennotizuspto-grants-2015_02