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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510913Generated: October 25, 2026

(3,5-Difluorophenyl)boronic acid → 1-(6-Bromo-4-chloro-3',5'-difluorobiphenyl-2-yl)ethanone

https://huagongshe.com/reaction/510913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,5-Difluorophenyl)boronic acidHCID 2734338—
ReactantSodiumHCID 5360545—
Reactant2-Acetyl-6-bromo-4-chlorophenyl trifluoromethanesulfonateHCID 86666832—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(6-Bromo-4-chloro-3',5'-difluorobiphenyl-2-yl)ethanoneHCID 6796927289.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of sodium hydrogenecarbonate (2.0 g, 23 mmol) in water (50 mL) was treated with a solution of 2-acetyl-6-bromo-4-chlorophenyl trifluoromethanesulfonate (4.5 g, 12 mmol) in toluene (50 mL) followed by (3,5-difluorophenyl)boronic acid (2.0 g, 13 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.67 g, 0.58 mmol). The reaction mixture was degassed with nitrogen for 5 min and heated at 80° C. overnight. The reaction mixture was diluted with water and extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with sodium bicarbonate, water, and brine, dried with sodium sulfate, filtered, and concentrated to a crude residue. Purification by flash column chromatography using ethyl acetate in hexanes (0%-10%) gave the desired product (3.7 g, 82%). LCMS for C14H9BrClF2O (M+H)+: m/z=344.9, 346.9. Found: 344.9, 346.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-d0747f37c2e0470a905b96db01b1c0a7
Source noteuspto-grants-2015_08