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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019563Generated: October 30, 2026

Ethanol → 2-Amino-5-fluoro-3-iodopyridine

https://huagongshe.com/reaction/1019563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodineHCID 807—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
CatalystHCID 178418844HCID 178418844—
SolventEthyl AcetateHCID 8857—
SolventSodium CarbonateHCID 10340—
Product2-Amino-5-fluoro-3-iodopyridineHCID 1845597425.2%

Reaction Steps

5 g (44.6 mmol) of 2-amino-5-fluoropyridine, 13.9 g (44.6 mmol) of silver sulfate and 400 mL of ethanol are put in a 500-mL two-necked flask equipped with a magnetic stirrer. Then 11.31 g (44.6 mmol) of iodine powder is added, in small portions. It is stirred at room temperature for 24 hours. The insoluble matter is removed by filtration and is washed with ethanol, and the filtrate is concentrated at reduced pressure. The residue thus obtained is taken up in a mixture of ethyl acetate (200 mL) and sodium carbonate solution (200 mL). After separation, the organic phase is washed successively with a 25% aqueous solution of sodium thiosulfate then with a saturated aqueous solution of sodium chloride, then it is dried over sodium sulfate and concentrated at reduced pressure. The resultant solid is purified by chromatography on a silica column, eluting with a mixture of n-heptane and ethyl acetate. We obtain 2.67 g (11.22 mmol) of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716273B2
Source datasetuspto-grants-2014_05
ORD IDord-fbd2751ed3c84993bd3d8a306d1b2d8f
Source noteuspto-grants-2014_05