HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595275Generated: November 3, 2026
Sodium Iodide → 4-(1-Fluoroethyl)-2-iodopyridine
https://huagongshe.com/reaction/595275
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Chloro-4-(1-fluoroethyl)pyridine | HCID 88878787 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(1-Fluoroethyl)-2-iodopyridine | HCID 118208903 | — |
Reaction Steps
2-Chloro-4-(1-fluoroethyl)pyridine (70 g, 439 mmol, 1.00 equiv), NaI (661 g, 4.41 mol, 10.00 equiv), ACN (700 mL) and acetyl chloride (56 g, 713 mmol, 1.60 equiv) were combined in a 2000-mL 4-necked round-bottom flask. The resulting solution was stirred overnight at 80° C. in an oil bath and then cooled to r.t, diluted with ice aqueous saturated sodium carbonate (500 mL) and extracted with dichloromethane (3×500 mL). The combined organic layer was washed with NaS2O3 (10%, 3×300 mL) and the aqueous phase was extracted with dichloromethane (2×200 mL). The combined organic layer was washed with brine (2×500 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by column chromatography on silica gel column (1:10 ethyl acetate/petroleum ether) to afford 4-(1-fluoroethyl)-2-iodopyridine as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242984B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-53b58e20354b40bc9963f7e0723fc49d |
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| Source note | uspto-grants-2016_01 |
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