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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-Chloro-3-fluoropicolinamide | HCID 22013575 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-Chloro-3-fluoropyridine-2-carbonitrile | HCID 22013562 | 91.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204221B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-46d03c38d9214db8b7084315d5a3fa9b |
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| Source note | uspto-grants-2001_03 |
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