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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464131Generated: October 25, 2026

Hydrochloric Acid → 3,6-Dichloro-5-trifluoromethyl-2-pyridone

https://huagongshe.com/reaction/464131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant2,3,6-Trichloro-5-(trifluoromethyl)pyridineHCID 2760690—
Solventtert-ButanolHCID 6386—
Product3,6-Dichloro-5-trifluoromethyl-2-pyridoneHCID 13491776—
Product5,6-Dichloro-3-trifluoromethyl-2-pyridoneHCID 13491777—

Reaction Steps

To a solution of 2.7 g of potassium hydroxide dissolved in 37 ml of t-butanol was added 6.0 g of 2,3,6-trichloro-5-trifluoromethylpyridine, and the solution was reacted at 80° C. for 3 hours while stirring. After completion of the reaction, the reaction product was allowed to cool and made acidic with concentrated hydrochloric acid. The solvent was distilled off under reduced pressure, and the residue was extracted with methylene chloride. The methylene chloride solution was washed with water and dried over anhydrous sodium sulfate. The methylene chloride was distilled off under reduced pressure, and the resulting residue was passed through a silica gel column (eluent: an n-hexane-ethyl acetate (3:1 by weight) mixture) to obtain 1.5 g of 3,6-dichloro-5-trifluoromethyl-2-pyridone having a melting point of 129° to 131° C. and 0.8 g of 5,6-dichloro-3-trifluoromethyl-2-pyridone having a melting point of 163° to 165° C., respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546191
Source datasetuspto-grants-1985_10
ORD IDord-c73373fb0e594425b6e2b10ff428bd3d
Source noteuspto-grants-1985_10