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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192588Generated: November 2, 2026

Nitrogen → 6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1192588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantWaterHCID 962—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant6-Acetyl-4-chloro-2-cyano-3-methylphenyl trifluoromethanesulfonateHCID 58368644—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventSodiumHCID 5360545—
Product6-Acetyl-4-chloro-3'-fluoro-3-methylbiphenyl-2-carbonitrileHCID 5836846999%

Reaction Conditions

Temperature80 °C

Reaction Steps

A biphasic solution of 6-acetyl-4-chloro-2-cyano-3-methylphenyl trifluoromethanesulfonate (2.537 g, 7.425 mmol) and (3-fluorophenyl)boronic acid (1.56 g, 11.1 mmol) in toluene (70 mL) and 0.8 M sodium hydrogenecarbonate in water (70 mL, 50 mmol) was bubbled with N2 to degas. Tetrakis(triphenylphosphine)palladium(0) (0.429 g, 0.371 mmol) was added. The mixture was degassed with N2 for an additional 5 minutes and then heated at 80° C. for 2 hours. After cooling to room temperature, the mixture was diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated to a dark solid. The material was dissolved in CHCl3 and was purified on silica gel column, eluting with 0 to 40% ethyl acetate in hexane, to give the desired product (2.105 g, 99%). LCMS calculated for C16H12ClFNO (M+H)+: m/z=288.1; Found: 288.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-ba713af4df3e4da482ee9891e20427fb
Source noteuspto-grants-2014_03