Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369627Generated: October 25, 2026

2-Chlorobenzonitrile → 2-Cyano-4'-methylbiphenyl

https://huagongshe.com/reaction/369627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzonitrileHCID 13391—
ReactantTolylboronic acidHCID 79799—
ReactantPotassium FluorideHCID 522689—
ReactantSodium 3,3',3''-phosphinetriyltribenzenesulfonate hydrateHCID 53487040—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethyl SulfoxideHCID 679—
SolventGlycerolHCID 753—
SolventWaterHCID 962—
SolventP-XyleneHCID 7809—
Product2-Cyano-4'-methylbiphenylHCID 14551286.4%

Reaction Steps

15 g of 2-chlorobenzonitrile, 15.8 g of p-tolueneboronic acid and 15.8 g of potassium fluoride in 50 ml of p-xylene, 40 ml of glycerol and 10 ml of water were heated to 120° C. At 80° C., a mixture of 24.7 mg of palladium acetate and 0.55 ml of TPPTS/H2O solution (0.6 molar) in 2.5 ml of DMSO was added. After the reaction was complete, the phases were separated. The aqueous phase was washed with 50 ml of toluene. The combined organic phases were washed with 20 ml of water and subsequently dried over sodium sulfate. Crystallization from n-heptane gave 18.2 g of 2-cyano-4'-methylbiphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140265
Source datasetuspto-grants-2000_10
ORD IDord-9663dec4e0784817bf060005278388b6
Source noteuspto-grants-2000_10