HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624301Generated: November 2, 2026
Sodium Iodide → 2-Iodo-4-[3-(trifluoromethoxy)phenyl]pyridine
https://huagongshe.com/reaction/624301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 2-Chloro-4-(3-(trifluoromethoxy)phenyl)pyridine | HCID 89649781 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Iodo-4-[3-(trifluoromethoxy)phenyl]pyridine | HCID 89649378 | 107% |
Reaction Steps
Acetyl chloride (4.45 mL, 62.6 mmol) was added to a solution of 2-chloro-4-[3-(trifluoromethoxy)phenyl]-pyridine [CAS 1261856-64-7] (11.42 g, 41.73 mmol) and sodium iodide (31.28 g, 208.67 mmol) in MeCN (200 mL) under N2, and the resulting suspension was heated at 80° C. for 18 hrs. Additional sodium iodide was added (20 mol %) and stirring was continued for 3 hrs. The reaction was cooled and the mixture was treated with aqueous sodium carbonate. After 5 minutes, solid sodium metabisulphite was added until decolourisation achieved. Water was added to redissolve a precipitate which had formed. The mixture was diluted with EtOAc and the layers separated. The aqueous layer was washed with EtOAc (2×), the combined organics were dried (MgSO4) and the solvent evaporated to afford the crude 2-iodo-4-[3-(trifluoromethoxy)phenyl]pyridine (D9) (16.3 g) as a amber oil containing about ˜5% of reduced 2-H material and ˜8% of unreacted chloride starting material;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303032B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-cc585df640b14d5da4ce1e9fc10df379 |
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| Source note | uspto-grants-2016_04 |
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