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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649288Generated: October 30, 2026

Water → HCID 14100540, compound

https://huagongshe.com/reaction/649288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 14100540HCID 14100540—

Reaction Steps

2,3-Dichloro-5-(trifluoromethyl)pyridine (43.2 g, 0.20 mole) was dissolved in 140 g (1.17 mole) of chloroform and 105 g of N-methylpyrrolidone. Sodium hydroxide (40 g of 50 percent aqueous solution, 0.5 mole) was added with stirring and the mixture was allowed to stir for 20 hours at room temperature. Another 10 g of 50 percent aqueous sodium hydroxide was added and stirring was continued. After 27 total hours a large excess of water was added. The resulting aqueous layer was removed and the organic layer was concentrated on a rotary evaporator under reduced pressure to obtain an oil containing the title compound. The oil was distilled in a fractionating column and the product fractions washed with dilute aqueous sodium carbonate to obtain 18.8 g of the title compound (35.5 percent of theory) having 97 percent purity by gas chromatography. The product, which was identified by its mass spectrum (parent peak at 263 mass units) and gas chromatographic parameters (compared with an authentic standard), had a boiling point of 108°-114° C. at 19 mm Hg pressure. Approximately 17.5 g of unreacted 2,3-dichloro-5-(trifluoromethyl)pyridine was also recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04739070
Source datasetuspto-grants-1988_04
ORD IDord-52be1d7d0bf74e86b388068af42b9e52
Source noteuspto-grants-1988_04