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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413953Generated: November 3, 2026

4-Bromobiphenyl → HCID 20291240, compound

https://huagongshe.com/reaction/1413953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobiphenylHCID 7101—
Reactant1,2-DibromoethaneHCID 7839—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-BenzoylpyridineHCID 26731—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20291240HCID 20291240—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 111.0 g (0.50 mole) of 4-biphenyl bromide in 200 ml of dry tetrahydrofuran (THF) was added slowly to a mixture of 12.10 g (0.5 gram-atom) of magnesium, 2 ml of ethylenedibromide and 200 ml of THF at such a rate as to maintain reflux. After addition the mixture was refluxed for 0.5 hours, cooled and treated over 0.5 hours with a solution of 82.3 g (0.45 mole) of 4-benzoylpyridine in 600 ml THF. The resulting slurry was stirred 0.5 hours at 25° C. and treated with 1000 ml 20% ammonium chloride solution. The organic layer was separated, filtered, the filtrate dried, filtered and stripped. The residue was triturated with ether and filtered. This solid was recrystallized from ethanol, chloroform, and finally toluene to give α-(1,4'-biphenyl)-yl-α-phenyl-4-pyridinemethanol as a white solid, m.p. after drying in vacuo at 70° C.; 173.5°-175.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251655
Source datasetuspto-grants-1981_02
ORD IDord-c02db72ba55f452c83a050332f318c0b
Source noteuspto-grants-1981_02