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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510819Generated: November 1, 2026

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

https://huagongshe.com/reaction/510819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant6-Acetyl-4-chloro-2-cyano-3-methylphenyl trifluoromethanesulfonateHCID 58368644—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
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 (2.54 g, 7.4 mmol) and (3-fluorophenyl)boronic acid (1.6 g, 11 mmol) in toluene (70 mL) and saturated sodium bicarbonate (70 mL) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (0.43 g, 0.37 mmol) was added, the mixture was bubbled with N2 for 5 min more and then heated at 80° C. for 2 hours. After cool to room temperature, the mixture was diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with more ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified on silica gel column, eluting with 0 to 40% ethyl acetate in hexane, to give the desired product (2.1 g, 99%). LCMS calculated for C16H12ClFNO (M+H)+: m/z=288.1. found: 288.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-900856663b4b420ca7875ac472ae52b9
Source noteuspto-grants-2015_08