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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantEthyl 5-chloronicotinateHCID 210009—
ReactantEthyl 5,6-DichloronicotinateHCID 16762519—
SolventPropionitrileHCID 7854—
ProductEthyl 5-chloro-6-iodo-3-pyridinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097628B2
Source datasetuspto-grants-2012_01
ORD IDord-dbb2593184944ecbab383f1ce7f8949b
Source noteuspto-grants-2012_01