HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357559Generated: November 1, 2026
N-Iodosuccinimide → 5-iodo-2-butoxynicotinic acid
https://huagongshe.com/reaction/1357559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 22667896 | HCID 22667896 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Trifluoroacetic anhydride | HCID 9845 | — |
| Product | 5-iodo-2-butoxynicotinic acid | HCID 11558796 | 68% |
Reaction Steps
N-Iodosuccinimide (6.0 g, 26.7 mmol) was added to a solution of 2-n-butoxypyridine-3-carboxylic acid (Preparation 4; 3.46 g, 17.7 mmol) in trifluoroacetic acid (28 mL) and trifluoroacetic anhydride (7 mL) and the reaction heated under reflux in the absence of light, for 3 hours. The cooled reaction mixture was concentrated under reduced pressure and the residue dissolved in ethyl acetate. This solution was washed sequentially with water (2×), aqueous sodium thiosulfate solution, aqueous sodium citrate solution, 2 N hydrochloric acid, and brine, then dried (MgSO4) and evaporated under reduced pressure. The solid was triturated with pentane, filtered, washed with additional pentane and dried, to give the title compound as a white solid (3.86 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06593332B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-c59d54c86e0e4bcc8b0631c4b94c56b9 |
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| Source note | uspto-grants-2003_07 |
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