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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019534Generated: October 27, 2026

Iodine → 2-Iodo-6-(trifluoromethyl)pyridin-3-amine

https://huagongshe.com/reaction/1019534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant5-Amino-2-(trifluoromethyl)pyridineHCID 2737744—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
Product2-Iodo-6-(trifluoromethyl)pyridin-3-amineHCID 5342547965.8%

Reaction Steps

1.56 g (6.17 mmol) of iodine is added, in several portions, to a mixture, stirred under argon at 20° C., of 1 g (6.17 mmol) of 3-amino-6-trifluoromethylpyridine and 1.25 g (6.17 mmol) of silver sulfate in 40 mL of ethanol. Stirring is maintained for 18 hours. The insoluble matter is removed by filtration and is washed with ethanol, the filtrate is concentrated at reduced pressure, and the residue is taken up in 100 mL of dichloromethane. The organic phase is washed successively with 20 mL of 5% aqueous solution of sodium hydroxide, 40 mL of water and 20 mL of saturated aqueous solution of sodium chloride, dried over sodium sulfate, concentrated at reduced pressure, and then purified by chromatography on a silica column (eluents: heptane-ethyl acetate). In this way we isolate 1.17 g of the expected product, which is used as it is in the rest of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716272B2
Source datasetuspto-grants-2014_05
ORD IDord-092935c3ee5e47278c8e8006fa12f543
Source noteuspto-grants-2014_05