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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354956Generated: October 26, 2026

1-Chloro-3,5-dimethoxybenzene → 3-Acetyl-3',5'-dimethoxybiphenyl

https://huagongshe.com/reaction/1354956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-3,5-dimethoxybenzeneHCID 81502—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178419130HCID 178419130—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Product3-Acetyl-3',5'-dimethoxybiphenylHCID 2221840591%

Reaction Steps

An oven dried Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), 3,5-dimethoxyphenyl chloride (173 mg, 1.0 mmol), 3-acetylphenylboron dihydroxide (246 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The reaction 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 ethyl acetate (30 mL) and poured into a separatory funnel. The mixture was washed with 2.0 M NaOH (20 mL). The organic layer was washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 232 mg (91%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223879B2
Source datasetuspto-grants-2007_05
ORD IDord-9421284a64ce459d97ea23483cfb7492
Source noteuspto-grants-2007_05