Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402594Generated: November 1, 2026

Iodine → 2-Amino-5-chloro-3-iodopyridine

https://huagongshe.com/reaction/402594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantMetaperiodic acidHCID 65185—
Reactant2-Amino-5-chloropyridineHCID 66174—
SolventAcetic acid--water (1/1)HCID 21899381—
Product2-Amino-5-chloro-3-iodopyridineHCID 11076010—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixed solution of 2-amino-5-chloropyridine (2.6 g, 0.020 mol) in acetic acid/water (7.8 mL/1.8 mL) that cooled with ice bath, conc.sulfuric acid (0.26 mL, 4.9 mmol) was added dropwise, and then periodic acid (0.95 g, 4.2 mmol) and iodine (2.0 g, 8.0 mmol) were added. The reaction mixture was stirred at 80° C. for 6 h. Cooled to ambient temperature, the reaction mixture was poured into ice water, and neutralized by aqueous 5M sodium hydroxide solution. After removal of the precipitate by filtration, the filtrate was extracted with ethyl acetate. The organic layer was washed with saturated sodium thiosulfate solution, aqueous 1M sodium hydroxide solution and brine then dried over sodium sulfate and concentrated to afford 2-amino-5-chloro-3-iodopyridine as solid (4.4 g, y. 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-b68ec7662cf94ca8a0c367402bd1b17a
Source noteuspto-grants-2014_06