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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578599Generated: October 25, 2026

Ethanol → 2-(biphenyl-2-yl)-7-bromo-9,9-dimethyl-9H-fluorene

https://huagongshe.com/reaction/578599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantBiphenyl-2-boronic acidHCID 4589187—
Reactant2,7-Dibromo-9,9-dimethylfluoreneHCID 12123876—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(biphenyl-2-yl)-7-bromo-9,9-dimethyl-9H-fluoreneHCID 5762287663%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 35.2 g (100 mmol) of 2,7-dibromo-9,9-dimethyl-9H-fluorene, 21.8 g (110 mmol) of biphenyl-2-ylboronic acid, 2.31 g (2 mmol) of Tetrakis(triphenylphosphine)palladium, 75 ml of 2M Na2CO3, 150 ml of EtOH and 300 ml toluene was degassed and placed under nitrogen, and then heated at 100° C. for 12 h. After finishing the reaction. The mixture was allowed to cool to room temperature. The organic layer was extracted with ethyl acetate and water, dried with anhydrous magnesium sulfate, the solvent was removed and the residue was purified by column chromatography on silica (hexane-dichloromethane) to give product (26.8 g, 63.0 mmol, 63%) as a white solid. 1H NMR (CDCl3, 400 MHz): δ 7.61 (d, J=7.8 Hz, 1H), 7.55˜7.53 (m, 2H), 7.49˜7.42 (m, 5H), 7.29 (d, J=8.0 Hz, 1H), 7.20˜7.14 (m, 5H), 6.98 (s, 1H), 1.21 (s, 6H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040174B2
Source datasetuspto-grants-2015_05
ORD IDord-524a22c7898446ee9df4c0ed23cf42d6
Source noteuspto-grants-2015_05