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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227854Generated: October 26, 2026

4-Chloroanisole → 4-Methoxybiphenyl

https://huagongshe.com/reaction/227854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanisoleHCID 12167—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 178419127HCID 178419127—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthylHCID 4368621—
Solvent1,4-DioxaneHCID 31275—
Product4-MethoxybiphenylHCID 1194394.2%

Reaction Steps

An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 0.5 mol %), ligand 2 [Example 1] (5.9 mg, 0.015 mmol, 0.75 mol %), phenylboron dihydroxide (366 mg, 3.0 mmol), and potassium phosphate (850 mg, 4.0 mmol). The tube was purged with argon, and dioxane (6 mL), and 4-chloroanisole (0.24 mL, 2.0 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 for two minutes, then heated to 100° 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 (40 mL) and poured into a separatory funnel. The mixture was washed with 1M NaOH (40 mL), and the layers were separated. The aqueous layer was extracted with ether (40 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 347 mg (94%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560582B2
Source datasetuspto-grants-2009_07
ORD IDord-9a94bd1a2b484dd5b18da8004731f986
Source noteuspto-grants-2009_07