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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862483Generated: October 25, 2026

Hydrogen Bromide → 2-Bromo-5-iodo-3-nitropyridine

https://huagongshe.com/reaction/1862483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Amino-5-iodo-3-nitropyridineHCID 3384468—
ReactantSodium NitriteHCID 23668193—
Product2-Bromo-5-iodo-3-nitropyridineHCID 1861978523%

Reaction Steps

5-iodo-3-nitro-2-aminopyridine (5.6 g, 21.1 mmol) and concentrated HBr (60 mL) were stirred at room temperature for ten minutes. Sodium nitrite (11.7 g, 170 mmol) was then slowly added followed by CuBr (3.9 g, 27.2 mmol). Stirring continued overnight. The mixture was poured into 1:1 NH4OH:H2O, extracted with ethyl acetate, dried over sodium sulfate, then concentrated. The crude residue was purified by flash chromatography using 9:1 hexane:ethyl acetate to yield 5-iodo-3-nitro-2-bromopyridine (1.618 g, 23%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06538010B1
Source datasetuspto-grants-2003_03
ORD IDord-f78044010f6442b0af80827b95acd521
Source noteuspto-grants-2003_03