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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097261Generated: October 29, 2026

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

https://huagongshe.com/reaction/1097261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantIodineHCID 807—
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
CatalystHCID 178418844HCID 178418844—
SolventEthyl AcetateHCID 8857—
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 sulphate and 400 ml of ethanol are introduced into a 500 ml two-necked flask equipped with a magnetic stirrer. 11.31 g (44.6 mmol) of powdered iodine are subsequently added in small portions. The stirring is continued at ambient temperature for 24 hours. The insoluble material is removed by filtration and washed with ethanol and the filtrate is concentrated under reduced pressure. The residue thus obtained is taken up in a mixture of ethyl acetate (200 ml) and of a solution of sodium carbonate (200 ml). After separation, the organic phase is washed successively with a 25% aqueous solution of sodium thiosulphate and then with a saturated aqueous solution of sodium chloride, and then dried over sodium sulphate and concentrated under reduced pressure. The resulting solid is purified by silica column chromatography, elution being carried out with a mixture of n-heptane and ethyl acetate. 2.67 g (11.22 mmol) of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143248B2
Source datasetuspto-grants-2012_03
ORD IDord-d92398f246ea49e39db1cb08f563cf40
Source noteuspto-grants-2012_03