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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183786Generated: October 31, 2026

Potassium Phosphate, Tribasic → 1-(6-Methylpyridin-3-yl)-2-(4-(methylsulfonyl)phenyl)ethanone

https://huagongshe.com/reaction/1183786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Bromo-4-(methylsulphonyl)benzeneHCID 77014—
Reactant3-Acetyl-6-methylpyridineHCID 95292—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product1-(6-Methylpyridin-3-yl)-2-(4-(methylsulfonyl)phenyl)ethanoneHCID 9925991—

Reaction Conditions

Temperature25 °C

Reaction Steps

1-(6-methylpyridin-3-yl)ethanone 1 (50 g, 370 mmol), 1-bromo-4-(methylsulfonyl)benzene 2 (87 g, 370 mmol), potassium phosphate (235.6 g, 3 equiv, 1.11 mol), palladium(II) acetate (125 mg, 0.15mol, 557 μmol), Xantphos (161 mg, 0.075% mol, 278 μmol) and N,N′-dimethylformamide (300 ml, 6 vol) were introduced in the order into a 2000 ml flask provided with mechanical stirring, thermometer and coolant, at 25° C. and under a nitrogen atmosphere. The reaction mixture was stirred at 25° C. and subject to three cycles of vacuum and nitrogen, then it was heated to 85° C. and stirred at such temperature for 27 h. The reaction mixture was then quenched to 45° C. and the stirring was stopped, promoting the separation of an aqueous phase that was removed by suction siphoning with the aid of vacuum. The resulting higher mixture was diluted with water (600 ml, 12 vol) and was quenched to 3° C. After 2 h stirring at such temperature, the resulting suspension was filtered and the product was washed with water (4×200 ml, 4×4 vol) and dried at 60° C. in vacuum, yielding the raw 1-(6-methylpyridin-3-yl)-2-[4-(methylsulfonyl)phenyl]ethanone of formula (I) (89.1 g, 83.2%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664402B2
Source datasetuspto-grants-2014_03
ORD IDord-fda5f8b69e74467ba2c32fae7c447b66
Source noteuspto-grants-2014_03