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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753707Generated: October 25, 2026

Ethanol → 2-(biphenyl-2-yl)-7-(5-methoxybiphenyl-2-yl)-9-phenyl-9H-carbazole

https://huagongshe.com/reaction/1753707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantBiphenyl-2-boronic acidHCID 4589187—
Reactant2-bromo-7-(5-methoxybiphenyl-2-yl)-9-phenyl-9H-carbazoleHCID 86730004—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(biphenyl-2-yl)-7-(5-methoxybiphenyl-2-yl)-9-phenyl-9H-carbazoleHCID 8673000558%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 3 g (5.9 mmol) of 2-bromo-7-(5-methoxybiphenyl-2-yl)-9-phenyl-9H-carbazole, 1.5 g (7.7 mmol) of biphenyl-2-ylboronic acid, 0.12 g (0.1 mmol) of tetrakis(triphenylphosphine)palladium, 15 ml of 2M Na2CO3, 20 ml of EtOH and 60 ml toluene was degassed and placed under nitrogen, and then heated at 110° C. for 8 h. After finishing the reaction, the mixture was allowed to cool to room temperature. The reaction mixture was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was evaporated in vacuum. The residue was purified by column chromatography on silica(hexane-dichloromethane) afforded a white solid (2 g, 3.4 mmol, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09166177B2
Source datasetuspto-grants-2015_10
ORD IDord-5a645e85bd604e518f29d1d4a6905f46
Source noteuspto-grants-2015_10