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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434635Generated: October 26, 2026

Iodine → 2-Amino-5-iodo-3-nitropyridine

https://huagongshe.com/reaction/1434635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantSodium ThiosulfateHCID 24477—
Reactant3-Nitropyridin-2-ylamineHCID 77887—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Amino-5-iodo-3-nitropyridineHCID 3384468193.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-amino-3-nitropyridine (5.0 g, 35.9 mmol), acetic acid (22 mL), water (5 mL), sulfuric acid (0.650 mL), and HIO4×2H2O (1.7 g, 7.5 mmol) was allowed to stir at 90° C. for 10 min. Iodine crystals (3.7 g, 14.6 mmol) were added in portions. After stirring for 1 h, the reaction was poured into saturated sodium thiosulfate and extracted with ethyl acetate. The organic layers were washed with 0.1 M NaOH and saturated brine, dried with sodium sulfate, then evaporated to give orange solid (7.5 g, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615567B2
Source datasetuspto-grants-2009_11
ORD IDord-fffef87291884d818b0849cb29e0c2af
Source noteuspto-grants-2009_11