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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382089Generated: October 26, 2026

P-Chloroacetophenone → 1-(3'-Methyl[1,1'-biphenyl]-4-yl)ethanone

https://huagongshe.com/reaction/382089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ChloroacetophenoneHCID 7467—
ReactantCesium fluorideHCID 25953—
Reactant3-Tolylboronic acidHCID 2733950—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2,3',5-Trimethyl-1,1'-biphenylHCID 11041689—
Solvent1,4-DioxaneHCID 31275—
Product1-(3'-Methyl[1,1'-biphenyl]-4-yl)ethanoneHCID 511295493%

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 %), 3-methylphenylboronic acid (204 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL), and 4-chloroacetophenone (0.13 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 195 mg (93%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307087B1
Source datasetuspto-grants-2001_10
ORD IDord-082a34eed01047abb85f6381075a1d7b
Source noteuspto-grants-2001_10