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HRID 1795656Erstellt: 24. Oktober 2026

Benzene, 2-bromo-1,4-dimethyl- → 2,5-Dimethylbiphenyl

https://huagongshe.com/de/reaction/1795656

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzene, 2-bromo-1,4-dimethyl-HCID 11121—
EduktPhenylboronic AcidHCID 66827—
EduktPotassium FluorideHCID 522689—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2-(Di-tert-butylphosphino)biphenylHCID 2734215—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2,5-DimethylbiphenylHCID 52250682%

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-p-xylene (0.138 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 room temperature 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 149 mg (82%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07026498B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-216551e3cd3f4df2929d218af9319a46
Quellennotizuspto-grants-2006_04