HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420744Generated: October 30, 2026
Sodium Iodide → Ethyl 5-chloro-6-iodo-3-pyridinecarboxylate
https://huagongshe.com/reaction/420744
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | Ethyl 5-chloronicotinate | HCID 210009 | — |
| Reactant | Ethyl 5,6-Dichloronicotinate | HCID 16762519 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | Ethyl 5-chloro-6-iodo-3-pyridinecarboxylate | HCID 58001783 | — |
Reaction Steps
To a solution of ethyl 5,6-dichloro-3-pyridinecarboxylate (1.00 g, 4.54 mmol) in propionitrile (30 ml) stirred under nitrogen at room temperature was added sodium iodide (2.044 g, 13.63 mmol) and iodotrimethylsilane (0.784 ml, 4.54 mmol). After stirring for 30 min, solvent was evaporated to dryness. The obtained brown oil was dissolved in water and pH was adjusted to basic with 2N NaOH. The aqueous phase was extracted with DCM, dried over anhydrous MgSO4 and concentrated under reduced pressure. Purification by flash chromatography using Flashmaster II, a 10 g silica gel cartridge, and mixtures of DCM/MeOH as eluent afforded a mixture of final product and ethyl 5-chloro-3-pyridinecarboxylate. The mixture was repurification by flash chromatography using Flashmaster II, a 50 g Merck silica gel cartridge, and mixtures of DCM/MeOH as eluent afforded the expected product ethyl 5-chloro-6-iodo-3-pyridinecarboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097628B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-dbb2593184944ecbab383f1ce7f8949b |
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| Source note | uspto-grants-2012_01 |
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