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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192705Generated: November 2, 2026

Nitrogen → 1-(4-Chloro-3'-fluoro-5-methyl-6-nitrobiphenyl-2-yl)ethanone

https://huagongshe.com/reaction/1192705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant6-Acetyl-4-chloro-3-methyl-2-nitrophenyl trifluoromethanesulfonateHCID 86656185—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
Product1-(4-Chloro-3'-fluoro-5-methyl-6-nitrobiphenyl-2-yl)ethanoneHCID 8665618692.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A biphasic solution of 6-acetyl-4-chloro-3-methyl-2-nitrophenyl trifluoromethanesulfonate (3.00 g, 8.29 mmol) and (3-fluorophenyl)boronic acid (1.74 g, 12.4 mmol) in toluene (80 mL) and saturated NaHCO3 (80 mL) was bubbled with N2 to degas. Tetrakis(triphenylphosphine)palladium(0) (0.479 g, 0.415 mmol) was added The reaction mixture was bubbled with N2 for 5 minutes more and 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. The resulting material was purified on silica gel column, eluting with ethyl acetate/hexane, 0-30%, to give the desired product (2.35 g, 92%). LCMS calculated for C15H12ClFNO3 (M+H)+: m/z=308.0; Found: 308.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-4e7d489470184161905591129055cde9
Source noteuspto-grants-2014_03