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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625899Generated: October 30, 2026

Cerium(III) chloride → 5-Bromo-2-chlorophenyl 6-ethyl-3-pyridyl ketone

https://huagongshe.com/reaction/1625899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCerium(III) chlorideHCID 24636—
ReactantSodium BicarbonateHCID 516892—
ReactantTriethylaluminumHCID 16682930—
Reactant5-Bromo-2-chlorophenyl 6-bromo-3-pyridyl ketoneHCID 46930335—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-chlorophenyl 6-ethyl-3-pyridyl ketoneHCID 46930524—

Reaction Conditions

Temperature30 °C

Reaction Steps

5-Bromo-2-chlorophenyl 6-bromo-3-pyridyl ketone (3.2 g) from Reference Example 135-(2) was dissolved in tetrahydrofuran (80 ml), and added thereto were triethylaluminium (1.0 M hexane solution, 9.9 ml), tetrakis(triphenylphosphine)palladium(0) (570 mg) and cerium(III) chloride (7.3 g), and the mixture was stirred at 30° C. for 1.5 hours. The reaction mixture was diluted with methanol, and the reaction solution was basified with a saturated aqueous sodium hydrogen carbonate solution. The insoluble materials were filtered off and, the filtrate was extracted with ethyl acetate and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=99:1-85:15) to give 5-bromo-2-chlorophenyl 6-ethyl-3-pyridyl ketone (1.98 g) as a colorless solid. APCI-Mass m/Z 324/326 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-c2a76b2f07c14be89bdb805626d87be4
Source noteuspto-grants-2014_07