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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
ReactantSodium CarbonateHCID 10340—
ReactantSodium PyrosulfiteHCID 656671—
Reactant2-Chloro-4-(3-(trifluoromethoxy)phenyl)pyridineHCID 89649781—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-Iodo-4-[3-(trifluoromethoxy)phenyl]pyridineHCID 89649378107%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303032B2
Source datasetuspto-grants-2016_04
ORD IDord-cc585df640b14d5da4ce1e9fc10df379
Source noteuspto-grants-2016_04