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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382112Generated: October 26, 2026

Potassium Phosphate, Tribasic → 1-(2'-Methoxy[1,1'-biphenyl]-2-yl)ethanone

https://huagongshe.com/reaction/382112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantEthanone, 1-(2-chlorophenyl)-HCID 72864—
Reactant2-Methoxyphenylboronic acidHCID 2733958—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
SolventTolueneHCID 1140—
Product1-(2'-Methoxy[1,1'-biphenyl]-2-yl)ethanoneHCID 2221840689%

Reaction Conditions

Temperature65 °C

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 %), 2-methoxyphenylboronic acid (228 mg, 1.5 mmol), and potassium phosphate (425 mg, 2.0 mmol). The tube was evacuated and backfilled with argon, and toluene (3 mL) and 2′-chloroacetophenone (0.13 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was heated to 65° C. with stirring 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 201 mg (89%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307087B1
Source datasetuspto-grants-2001_10
ORD IDord-c6c50fa64d4e4dc3ad91b6565f6ba4f3
Source noteuspto-grants-2001_10