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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795664Generated: October 26, 2026

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

https://huagongshe.com/reaction/1795664

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 numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-4d0641dc216a413fa60465c63a55033b
Source noteuspto-grants-2006_04