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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795637Generated: November 4, 2026

4-Chlorotoluene → 4-Methylbiphenyl

https://huagongshe.com/reaction/1795637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorotolueneHCID 7810—
ReactantCesium fluorideHCID 25953—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 178419127HCID 178419127—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Product4-MethylbiphenylHCID 1256693%

Reaction Steps

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 (0.12 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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-31bae94f582f455dacdb668c1632db06
Source noteuspto-grants-2006_04