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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354928Generated: October 25, 2026

Cesium fluoride → 3,5-Dimethylbiphenyl

https://huagongshe.com/reaction/1354928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant1,4-DioxaneHCID 31275—
ReactantBenzene, 1-bromo-3,5-dimethyl-HCID 136357—
ReactantHCID 178419127HCID 178419127—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthylHCID 4368621—
Product3,5-DimethylbiphenylHCID 8692794%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223879B2
Source datasetuspto-grants-2007_05
ORD IDord-6b6f82dbd18641e4b252a2e734e4047b
Source noteuspto-grants-2007_05