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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884190Generated: November 2, 2026

3-Chloroanisole → 3-Methoxybiphenyl

https://huagongshe.com/reaction/1884190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanisoleHCID 17833—
ReactantCesium fluorideHCID 25953—
ReactantPhenylboronic AcidHCID 66827—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-MethoxybiphenylHCID 25797194%

Reaction Steps

A 100 mL of reactor equipped with magnetic stir bar was charged with 150 mg (0.161 mmol) of {[(t-Bu)2P(OH)]2PdCl}2 (from Experiment 7), 1.43 g (10.0 mmol) of 3-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 DME. The resulting mixture was refluxed for 12 h until the starting material was completely consumed as judged by TLC. The reaction was cooled to room temperature, transferred to a separatory funnel, and diluted with 300 mL of diethyl ether. 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 1.73 g (94% yield) of 3-phenylanisole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762330B2
Source datasetuspto-grants-2004_07
ORD IDord-10b0b8139e044e34811417d338c4b605
Source noteuspto-grants-2004_07