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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884194Generated: November 2, 2026

4-Chloroanisole → 4-Methoxybiphenyl

https://huagongshe.com/reaction/1884194

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanisoleHCID 12167—
ReactantCesium fluorideHCID 25953—
ReactantPhenylboronic AcidHCID 66827—
Solvent1,4-DioxaneHCID 31275—
Product4-MethoxybiphenylHCID 1194353%

Reaction Steps

A 100 mL of reactor equipped with magnetic stir bar was charged with 140 mg (0.15 mmol) of {[(t-Bu)2P(OH)]2PdCl}2 (from Experiment 7), 1.43 g (10.0 mmol) of 4-chloroanisole, 1.83 g (15.0 mmol) of PhB(OH)2 and 4.56 g (30.0 mmol) of CsF in 30.0 mL of 1,4-dioxane. The resulting mixture was refluxed for 8 h until the starting material was completely consumed as judged by GC. The reaction was cooled to room temperature, transferred to a separatory funnel, and diluted with 300 mL of diethyl ether and 100 mL of H2O. The layers were separated, and organic layer was washed with H2O (2×100 mL), brine (100 mL), and dried over mgSO4, filtered, and the ether and dioxane removed from the filtrate by rotary evaporation. The resulting residue was chromatographed on silicon gel using 2% EtOAc/hexane as eluant. The eluate was concentrated by rotary evaporation followed by high vacuum to give 0.97 g (53% yield) of 4-phenylanisole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762330B2
Source datasetuspto-grants-2004_07
ORD IDord-99b89c1da127425ba0fb0d2468611754
Source noteuspto-grants-2004_07