Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | HCID 178469094 | HCID 178469094 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl 6-hydroxy-5-iodonicotinate | HCID 178469850 | 83% |
Reaction Steps
Ethyl 6-hydroxynicotinate (2.0 g, 12.0 mmol) was dissolved in pyridine (60 mL), which was then added with iodide (6.07 g, 23.9 mmol) and stirred at 60° C. overnight. The reaction solution was then added with water at room temperature and extracted with ethyl acetate. Subsequently, the organic layer was washed with a saturated aqueous solution of sodium sulfite and brine, and dried over sodium sulfate. The obtained residue was purified using column chromatography (chloroform/methanol) and concentrated in vacuo. Ethyl 6-hydroxy-5-iodonicotinate (2.9 g, yield 83%) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153634B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-ca1f2f17b944479d9b6fe4e4f2acb72e |
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| Source note | uspto-grants-2012_04 |
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