HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534752Generated: October 29, 2026
Water → 5-Bromopyridine-2-carboxylic acid
https://huagongshe.com/reaction/534752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromopyridine-2-carbonitrile | HCID 817154 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromopyridine-2-carboxylic acid | HCID 608544 | — |
Reaction Steps
5-Bromo-2-pyridinecarbonitrile (1 g, 5.464 mmol) was dissolved in EtOH (20 mL) and water (20 mL) and treated with potassium hydroxide (1.53 g, 27.32 mmol). The reaction mixture was heated to 80° C. for 24 h. The solvent was removed under vacuum and the residue was taken up in water and acidified to pH 4 with 2M HCl. The aqueous layer was extracted with ethyl acetate (×3) and the combined organic layers dried and concentrated to give 5-bromo-2-pyridinecarboxylic acid (0.704 g) as an orange solid which was used in step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853218B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-362f332401674489971baeed68b4b02b |
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| Source note | uspto-grants-2014_10 |
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