HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113415Generated: November 2, 2026
Lithium Hydroxide → 4-Amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acid
https://huagongshe.com/reaction/2113415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylate | HCID 67026614 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acid | HCID 67026609 | 78.5% |
Reaction Steps
A solution of lithium hydroxide (0.49 g, 11.73 mmol) in water (25 mL) was added to a solution of methyl 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylate (1.36 g, 5.86 mmol) in tetrahydrofuran (25 mL). The mixture was vigorously stirred at room temperature overnight and was then concentrated to half volume. After adding water the reaction mixture was washed once with ethyl acetate to remove unreacted starting material. The aqueous layer was then acidified to pH<3 with 1N HCl, concentrated and the residue partitioned between tetrahydrofuran and brine. The aqueous layer was discarded and the organic layer concentrated and dried under vacuum to provide 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acid (1.01 g, 4.60 mmol) as a white solid, mp 144-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432227B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-447f19aa406c428fbf8a92b64913814b |
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| Source note | uspto-grants-2008_10 |
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