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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305261Generated: October 25, 2026

Bromobenzene → alpha-Phenyl[1,1'-biphenyl]-4-methanol

https://huagongshe.com/reaction/2305261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantAmmonium ChlorideHCID 25517—
Reactant(1,1'-Biphenyl)-4-carboxaldehydeHCID 76689—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Productalpha-Phenyl[1,1'-biphenyl]-4-methanolHCID 9551239.7%

Reaction Steps

A mixture of bromobenzene (0.3 mol) in THF (300 ml) was added dropwise to a mixture of magnesium (0.32 mol) in THF (20 ml). The mixture was stirred and refluxed for 1 hour. A mixture of 4-biphenylcarboxaldehyde (0.3 mol) in THF (500 ml) was added dropwise. The mixture was stirred and refluxed for 2 hours, at room temperature overnight, poured out into a saturated NH4Cl solution and extracted with DCM. The organic layer was separated, washed three times, dried, filtered and the solvent was evaporated. The residue was triturated in hexane, filtered off and purified over silica gel on a glass filter (eluent: CH2Cl2 100%). The pure fractions were collected and the solvent was evaporated. The residue was triturated in DIPE, filtered off and dried, yielding 31 g of (±)-α-phenyl(1,1′-biphenyl)-4-methanol (interm. 23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440440B1
Source datasetuspto-grants-2002_08
ORD IDord-e60be3078c484e729af67d107b00b8f3
Source noteuspto-grants-2002_08