HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529153Generated: November 4, 2026
Acetic Acid → 2-Chloro-5-fluoropyridine-3-carboxamide
https://huagongshe.com/reaction/1529153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2,6-Dichloro-5-fluoronicotinamide | HCID 2774022 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Chloro-5-fluoropyridine-3-carboxamide | HCID 12629796 | — |
Reaction Steps
At RT, 44 g (210.58 mmol) of 2,6-dichloro-5-fluoronicotinamide were added to a suspension of 21.9 g (335.35 mmol) of zinc in methanol (207 ml). Acetic acid (18.5 ml) was then added, and the mixture was heated at reflux with stirring for 24 h. The contents of the flask were then decanted off from the zinc, and ethyl acetate (414 ml) and saturated aqueous sodium bicarbonate solution (414 ml) were added, followed by extraction with vigorous stirring. Subsequently, the reaction mixture was filtered with suction through kieselguhr, and the filter cake was washed three times with ethyl acetate (517 ml each time). The organic phase was removed and the aqueous phase was washed with ethyl acetate (258 ml). The combined organic phases were washed once with saturated aqueous sodium bicarbonate solution (414 ml), dried and concentrated under reduced pressure. Dichloromethane (388 ml) was added to the solid obtained in this manner, and extraction was effected by stirring for 20 min. The mixture was once more filtered off with suction, and the filter cake was washed with diethyl ether and sucked dry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090610B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-9b3531eda91649f5a50a97c885acb6e8 |
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| Source note | uspto-grants-2015_07 |
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