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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350956Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 14303987, compound

https://huagongshe.com/reaction/2350956

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,6-DifluoroanilineHCID 79647—
ReactantHCID 19847698HCID 19847698—
SolventO-XyleneHCID 7237—
ProductHCID 14303987HCID 1430398724.5%

Reaction Steps

In 200 ml of xylene were dissolved 6.3 g (0.020 mole) of 5-(2-chlorophenyl)-2-methyl-1-phenyl-1,3,5-pentanetrione, 20.0 g (0.155 mole) of 2,6-difluoroaniline, 4,6 g (0.024 mole) of para-toluenesulfonic acid and 50.0 g of Molecular Sieves 5A, followed by reflux for 8 hours. Solid matter was filtered off from the reaction mixture and 300 ml of chloroform was added to the filtrate. The mixture obtained was washed first with 50 ml of 10% aqueous solution of sodium hydroxide. After washing the chloroform layer further with water, it was dried over anhydrous sodium sulfate. Subsequent to removal of the sodium sulfate, the solvent was distilled off and the residue was subjected to column chromatography (eluent: ethyl acetate) to afford crystals. The crystals were recrystallized from a 2:1 mixed solvent of acetone and hexane, thereby yielding 2.0 g of 6-(2-chlorophenyl)-1-(2,6-difluorophenyl)-3-methyl-2-phenyl-4(1H)-pyridinone having a melting point of 213°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871751
Source datasetuspto-grants-1989_10
ORD IDord-a9a2ec8805ee4ebf9c0fc275f5896803
Source noteuspto-grants-1989_10