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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003988Generated: October 31, 2026

Phosphorus oxychloride → 2-Pyridone

https://huagongshe.com/reaction/1003988

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 numberUS06048823
Source datasetuspto-grants-2000_04
ORD IDord-b3973767a4e14682ac8004870c65639d
Source noteuspto-grants-2000_04