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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510855Generated: October 31, 2026

Nitrogen → 1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone

https://huagongshe.com/reaction/510855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPhenylboronic AcidHCID 66827—
Reactant6-Acetyl-2-bromo-4-chloro-3-methylphenyl trifluoromethanesulfonateHCID 86666786—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
Product1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanoneHCID 8666678793.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A biphasic solution of 6-acetyl-2-bromo-4-chloro-3-methylphenyl trifluoromethanesulfonate (3.3 g, 8.3 mmol) and phenylboronic acid (1.2 g, 10 mmol) in toluene (30 mL) and saturated sodium bicarbonate in water (30 mL) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (0.385 g, 0.333 mmol) was added, the mixture was bubbled with N2 for 5 min. more and heated at 80° C. for 2 hours. After cooling to r.t., 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 0-20% of ethyl acetate in hexane, to give the desired product (2.5 g, 93%). LCMS calculated for C15H13BrClO (M+H)+: m/z=323.0. found: 323.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-7a08fc72b71d4260ab77c88d1f5e3a76
Source noteuspto-grants-2015_08