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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700280Generated: October 26, 2026

3-Bromotoluene → 3'-Methyl[1,1'-biphenyl]-3-carbonitrile

https://huagongshe.com/reaction/1700280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromotolueneHCID 11560—
Reactant3-BromobenzonitrileHCID 23381—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product3'-Methyl[1,1'-biphenyl]-3-carbonitrileHCID 139397566.2%

Reaction Conditions

Temperature105 °C

Reaction Steps

A mixture of 3-bromobenzonitrile (910 mg), Pd(Ph3P)4 (290 mg), (Me3Sn)2 (1.64 g) and dioxane (20 mL) was sealed under argon in a pressure tube. The tube was then heated at 100-110° C. for 3 hours with stirring and another 15 hours at 80° C. To the reaction mixture was added 1-bromo-3-methylbenzene (940 mg), Pd(PPh3)4 (290 mg) and dioxane (5 mL) under argon. The sealed tube was heated at 135-140° C. with stirring for two days. The catalyst was filtered off and the filtrate was poured into water and extracted with ethyl acetate (3×). The organic layer was washed with brine, dried over Mg2SO4, concentrated and purified on silica gel column (ethyl acetate/hexane, 1:3) to afford 0.64 g of 3-(3-cyanophenyl)-1-methylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350761B1
Source datasetuspto-grants-2002_02
ORD IDord-7e7471371ef84ed6b5916003de8fd24f
Source noteuspto-grants-2002_02