Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 382088Erstellt: 25. Oktober 2026

4-Chlorotoluene → 4-Methylbiphenyl

https://huagongshe.com/reaction/382088

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-ChlorotolueneHCID 7810—
EduktCesium fluorideHCID 25953—
Edukt1,4-DioxaneHCID 31275—
EduktHCID 178419127HCID 178419127—
Katalysatorpalladium(II) acetateHCID 167845—
Katalysator2,3',5-Trimethyl-1,1'-biphenylHCID 11041689—
Produkt4-MethylbiphenylHCID 1256693%

Reaktionsschritte

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (4.4 mg, 0.02 mmol, 2 mol %), ligand 2 [Example 1] (11.9 mg, 0.03 mmol, 3 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 4-chlorotoluene (0.12mL, 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 chloride 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 157 mg (93%) of a glassy solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06307087B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-06a7ecd3c21141bab8176e97a9ba880f
Quellennotizuspto-grants-2001_10