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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795651Generated: October 27, 2026

Methyl 4-chlorobenzoate → 4-Carbomethoxy-3'-Acetylbiphenyl

https://huagongshe.com/reaction/1795651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chlorobenzoateHCID 14307—
ReactantPotassium FluorideHCID 522689—
Reactant3-Acetylphenylboronic acidHCID 2734310—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Product4-Carbomethoxy-3'-AcetylbiphenylHCID 432880490.1%

Reaction Steps

An oven dried resealable 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-acetylphenyl boronic acid (246 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and methyl-4-chlorobenzoate (171 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and 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 ether (30 mL) and poured into a separatory funnel. The mixture was washed with water (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were 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 229 mg (90%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-e0c4cc19fc8c428285b86f6704b0dbd9
Source noteuspto-grants-2006_04