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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496944Erstellt: 24. Oktober 2026

Phenylboronic Acid → 2,6-Dimethylbiphenyl

https://huagongshe.com/de/reaction/496944

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylboronic AcidHCID 66827—
Edukt2-Bromo-m-xyleneHCID 68471—
EduktPotassium FluorideHCID 522689—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-(Di-tert-butylphosphino)biphenylHCID 2734215—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,6-DimethylbiphenylHCID 13809079%

Reaktionsschritte

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-bromo-m-xylene (0.144 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at 65° C. until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 144 mg (79%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06946560B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-f614fd4d1e1a4e179b1cc44e44e05fda
Quellennotizuspto-grants-2005_09