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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269534Generated: October 25, 2026

Toluene → 2'-Benzyloxy-2-bromobiphenyl

https://huagongshe.com/reaction/269534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,2-DibromobenzeneHCID 11414—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-(Benzyloxy)phenyl)boronic acidHCID 2773253—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2'-Benzyloxy-2-bromobiphenylHCID 5873098969.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 2-benzyloxyphenylboronic acid (4.3 g. 19.3 mmol) and 1,2-dibromobenzene (9.11 g, 4.66 ml, 38.6 mmol) in 1:1 toluene:ethanol (150 ml) was stirred under nitrogen and tetrakis(triphenylphosphine)palladium(0) (1.12 g, 0.95 mmol) and potassium carbonate (21.3 g, 154 mmol) added. The reaction was stirred at 90° C. under nitrogen for 2 hours. After cooling, diethyl ether (100 ml) and water (100 ml) were added and the organic phase separated. The aqueous phase was extracted with diethyl ether (50 ml) and the combined organic layers washed with water, dried (MgSO4) and the solvent removed in vacuo. The residue was flash chromatographed (silica gel, 5-15% CH2Cl2-isohexane) to give the title compound as a clear oil (4.53 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446222B2
Source datasetuspto-grants-2008_11
ORD IDord-09e66ee2f0534b5281064bf3de981d67
Source noteuspto-grants-2008_11