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HRID 1847102Erstellt: 26. Oktober 2026

Pentafluoroiodobenzene → 2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenyl

https://huagongshe.com/reaction/1847102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentafluoroiodobenzeneHCID 70008—
Edukt2-(2-Methoxy-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 79662121—
KatalysatorTetrabutylammonium BromideHCID 74236—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
LösungsmittelPotassium CarbonateHCID 11430—
Produkt2,3,4,5,6-Pentafluoro-2'-methoxy-5'-methyl-1,1'-biphenylHCID 5732780393%

Reaktionsschritte

Compound 5 (11.3 g, 45.54 mmol, 1 equiv) and iodopentafluorobenzene (10.6 g, 36.2 mmol, 1 equiv) were dissolved in toluene (200 mL) and 1.0M potassium carbonate solution (200 mL). Tetrabutylammonium bromide (1.6 g, 5 mmol, 0.11 equiv) was added and the solution sparged with nitrogen for 10 minutes. Tetrakis(triphenylphosphine)palladium(0) (2.63 g, 2.28 mmol, 0.05 equiv) was added and the reaction was refluxed for one day. The reaction was cooled to room temperature, then the layers were separated. The aqueous phase was back extracted with ethyl acetate (2×200 mL). Combined organic phases were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified over silica gel (200 g), eluting with heptanes to give 2,3,4,5,6-pentafluoro-2′-methoxy-5′-methyl-1,1′-biphenyl (6) (9.7 g, 74% yield) as a pale-yellow oil. This material contained a small amount of unreacted iodopentafluorobenzene which was identified by 19F NMR. The material was used subsequently.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08952114B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-e95ef93340a349c391c502c27ec4471d
Quellennotizuspto-grants-2015_02