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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36822Generated: October 26, 2026

Benzene → 4-Methoxy-3-fluoro-4"-cyano-p-terphenyl

https://huagongshe.com/reaction/36822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium CarbonateHCID 10340—
Reactant4'-bromo-[1,1'-Biphenyl]-4-carbonitrileHCID 1394462—
Reactant3-Fluoro-4-methoxyphenylboronic acidHCID 2782194—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product4-Methoxy-3-fluoro-4"-cyano-p-terphenylHCID 2207962988.6%

Reaction Steps

To a mixture of 2.4 g of 4-bromo-4'-cyanobiphenyl, 0.37 g of tetrakis(triphenylphosphine)palladium(0), 15.2 ml of a 2N aqueous sodium carbonate solution, and 19.4 ml of benzene, a solution which was prepared by dissolving 1.9 g of 4-methoxy-3-fluoro-benzene boronic acid synthesized in [1] above in 14.4 ml of ethanol was slowly added dropwise with stirring, and the solution was subjected to reflux for 8 hours. After the reflux was finished, the solution was cooled, and the crystals thus precipitated were separated by filtration and washed with water and methanol in turn, and dried to obtain 2.5 g of 4-methoxy-3-fluoro-4"-cyano-p-terphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05417885
Source datasetuspto-grants-1995_05
ORD IDord-856c078c427a48308a9a01c4b78b789f
Source noteuspto-grants-1995_05