HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377813Generated: October 30, 2026
Potassium Iodide → 2-(2-tert-Butylphenoxy)-3-iodopyridine
https://huagongshe.com/reaction/2377813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2-(2-Tert-butylphenoxy)pyridin-3-amine | HCID 28605427 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-tert-Butylphenoxy)-3-iodopyridine | HCID 59857435 | 56% |
Reaction Steps
A solution of sodium nitrite (157 mg, 2.28 mmol) in water (1 mL) was added to a mixture of 2-(2-tert-butylphenoxy)-3-aminopyridine (prepared above according to 1b) (500 mg, 2.07 mmol) in (1:1) conc. HCl: water (14 mL) at 0° C. The mixture was stirred at 0° C. for 15 min and a solution of potassium iodide (1.0 g, 6.22 mmol) in water (2 mL) was added. The mixture was stirred at 60° C. for 1.5 h and allowed to cool down to rt. A solution of sodium bisulfite was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried (anhydrous sodium sulfate), filtered and evaporated. The residue was purified by flash-chromatography (dichloromethane:hexanes/20:100) to afford 394 mg (56%) of 2-(2-tert-butylphenoxy)-3-iodopyridine. (M+H)+=354.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07470712B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-8c9bbd5966a24a6e86aed3b3ccb78b3d |
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| Source note | uspto-grants-2008_12 |
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