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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532566Generated: October 27, 2026

Hydrochloric Acid → 5-Chloro-3-fluoropyridine-2-carbonitrile

https://huagongshe.com/reaction/1532566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Chloro-3-fluoropicolinamideHCID 22013575—
SolventPyridineHCID 1049—
Product5-Chloro-3-fluoropyridine-2-carbonitrileHCID 2201356291.5%

Reaction Steps

1.39 g of 3-fluoro-5-chloro-2-pyridinecarboxamide (Example H7) are initially introduced into 8 ml of absolute dioxane, and 1.3 ml of dry pyridine are added. 1.30 ml of trifluoroacetic anhydride are slowly added with a syringe, while stirring and cooling in an ice-bath, and the mixture is subsequently stirred for 30 minutes. The resulting reaction mixture is poured onto 1N hydrochloric acid at 25° C. and extracted with diethyl ether. The ether phase is washed with dilute hydrochloric acid, water, dilute sodium bicarbonate solution and water. After drying over sodium sulfate, the mixture is filtered and the filtrate is concentrated to dryness. 1.14 g of the desired compound are obtained as a slightly violet-coloured solid of melting point 72-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204221B1
Source datasetuspto-grants-2001_03
ORD IDord-46d03c38d9214db8b7084315d5a3fa9b
Source noteuspto-grants-2001_03