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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662917Generated: October 30, 2026

Toluene → 2-(4-Bromophenyl)-6-phenylnaphthalene

https://huagongshe.com/reaction/1662917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant(6-Phenylnaphthalen-2-yl)boronic acidHCID 57539613—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(4-Bromophenyl)-6-phenylnaphthaleneHCID 5753981173.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

Under an argon gas atmosphere, 20.0 g (70.7 mmol) of 4-bromoiodobenzene, 17.5 g (70.7 mmol) of 6-phenylnaphthalene-2-boronic acid, 1.63 g (1.41 mmol) of tetrakis(triphenylphosphine) palladium(0), 200 mL of toluene, 50 mL of dimethoxyethane and 107 mL of 2M sodium carbonate solution were mixed, and stirred for 10 hours at 90 degrees C. Subsequently, the reaction mixture was cooled down to room temperature, added with water and stirred for one hour. After the solid precipitated during the reaction was separated by filtration, the obtained solid was cleansed with water, methanol, dimethoxyethane and toluene in this order. By dissolving the obtained solid in toluene and refining the solution by silica-gel column chromatography, 18.6 g of 2-(4-bromophenyl)-6-phenylnaphthalene was obtained at an yield of 73%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034256B2
Source datasetuspto-grants-2011_10
ORD IDord-efe494dd18ed4cdbbef535cdf74e24c7
Source noteuspto-grants-2011_10