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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227851Erstellt: 25. Oktober 2026

Cesium fluoride → 3,5-Dimethylbiphenyl

https://huagongshe.com/reaction/227851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium fluorideHCID 25953—
Edukt1,4-DioxaneHCID 31275—
EduktBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
EduktHCID 178419127HCID 178419127—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthylHCID 4368621—
Produkt3,5-DimethylbiphenylHCID 8692794%

Reaktionsschritte

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1 mol %), ligand 2 [Example 1] (5.9 mg, 0.015 mmol, 1.5 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL) and 5-bromo-m-xylene (0.135 mL, 1.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the 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 (20 mL) and poured into a separatory funnel. The mixture was washed with 1M NaOH (20 mL), and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 171 mg (94%) of a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560582B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-03db3cf90ed441c4aa4f64d227ab0f4c
Quellennotizuspto-grants-2009_07