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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385954Generated: November 4, 2026

Phosphorus oxychloride → 2-Pyridone

https://huagongshe.com/reaction/1385954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(4-Chlorophenyl)-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyridineHCID 18408327—
SolventN,N-DiethylanilineHCID 7061—
Product2-PyridoneHCID 887137%
ProductPiridin-4-oneHCID 1798489729%

Reaction Conditions

Temperature110 °C

Reaction Steps

3.3 g (10.9 mmol) of 3-(4-chlorophenyl)-2,4-dioxo-1-methyl-6-trifluoromethyl-1,2,3,4-tetrahydropyridine was added to 8.3 g (42.3 mmol) of phosphorus oxychloride and 30 ml of diethylaniline, followed by stirring at from 100 to 120° C. for 4 hours. The reaction solution was distilled off under reduced pressure, and ethyl acetate was added to the obtained residue, followed by washing with water and a saturated sodium hydrogencarbonate aqueous solution. The organic layer was dried over anhydrous magnesium sulfate. The organic layer was distilled off under reduced pressure, and the obtained residue was separated and purified by high performance liquid chromatography to obtain 1.3 g (yield: 37%) of the desired 2-pyridone compound (Compound No. 11-1) and 1.0 g (yield: 29%) of the 4-pyridone compound (Compound No. 13-1), respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265349B1
Source datasetuspto-grants-2001_07
ORD IDord-dbf87c2a269d422c905fd4c84321c377
Source noteuspto-grants-2001_07