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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072753Generated: November 3, 2026

4-Bromo-o-xylene → Biphenyl

https://huagongshe.com/reaction/2072753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-o-xyleneHCID 68504—
ReactantMagnesiumHCID 5462224—
CatalystCupric ChlorideHCID 24014—
SolventTetrahydrofuranHCID 8028—
ProductBiphenylHCID 709550.8%

Reaction Steps

A solution of 13.7 g of 4-bromo-o-xylene in 50 ml of dry tetrahydrofuran is added dropwise to a suspension of magnesium filings (1.95 g) in 50 ml of dry tetrahydrofuran in the course of 1 hour. After refluxing in an argon atmosphere for 2 hours, the mixture is cooled to room temperature and 9.4 g of anhydrous copper(II) chloride are added in portions. The mixture is poured onto ice-water and extracted twice with 100 ml of diethyl ether each time. The organic phase is washed with 2N hydrochloric acid and saturated sodium chloride solution. Drying with magnesium sulfate, evaporation and crystallisation of the residue from ethanol gives 2.9 g of biphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914181
Source datasetuspto-grants-1990_04
ORD IDord-1cdf2cbd4ffc4713915ff90897113b92
Source noteuspto-grants-1990_04