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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466647Generated: October 29, 2026

1-Bromo-4-iodobenzene → 4'-Bromo-2-methyl-1,1'-biphenyl

https://huagongshe.com/reaction/466647

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-iodobenzeneHCID 11522—
ReactantHCID 178424303HCID 178424303—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4'-Bromo-2-methyl-1,1'-biphenylHCID 1520587682%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A stirred solution of 21.0 mL of (2-methylphenyl)magnesium bromide (42.0 mmol, 2.0M in diethyl ether) was evaporated in situ at room temperature. The syrupy residue was redissolved in 50 mL of THF and cooled to -20° C. under argon. To this solution was added a solution of 6.84 g (50.0 mmol) of thricefused zinc chloride. The resulting thick white slurry was warmed to room temperature and stirred for 1 hour. After cooling to -78° C., a solution of 11.32 g (40.0 mmol) of 1-bromo-4-iodobenzene and 500 mg (0.4 mmol) of tetrakis(triphenylphosphine)palladium in 50 mL of THF was added over the course of thirty minutes. After an additional 20 minutes, the cooling bath was removed, the reaction stirred at room temperature for 2 hours and then quenched with 100 mL of 1M hydrochloric acid. The mixture was extracted twice with hexanes, the extracts combined, washed once with saturated sodium bicarbonate solution and once with 10% sodium thiosulfate. The organic extract was dried (MgSO4) and evaporated. The crude product (11.3 g) was purified by distillation (bp 93°-95° C. at 0.5 Torr) to give 8.06 g (82%) of title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157027
Source datasetuspto-grants-1992_10
ORD IDord-d617cd918b464deabe1c3fe33495ba34
Source noteuspto-grants-1992_10