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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434641Generated: October 25, 2026

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

https://huagongshe.com/reaction/1434641

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 numberUS07615567B2
Source datasetuspto-grants-2009_11
ORD IDord-68c9d6171e4c4c63aa75cb8747ad4930
Source noteuspto-grants-2009_11