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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504484Generated: October 30, 2026

Sulfuric Acid → 2,3-Dichloro-5-iodo-6-methoxypyridine

https://huagongshe.com/reaction/1504484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
ReactantN-IodosuccinimideHCID 120273—
Reactant2,3-Dichloro-6-methoxypyridineHCID 3019245—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product2,3-Dichloro-5-iodo-6-methoxypyridineHCID 11773719876.1%

Reaction Steps

A RBF was charged with 2,3-dichloro-6-methoxypyridine (4.84 g, 27.2 mmol, Accel Pharmtech), DCM (40.0 ml), AcOH (40.0 ml), and sulfuric acid (0.797 ml, 14.95 mmol) to give a clear solution. N-iodosuccinimide (6.12 g, 27.2 mmol) was added in one portion to give a maroon-colored solution. The reaction was stirred for three hours at RT. The mixture was diluted with ethyl acetate, washed with water, washed with 10% aq. sodium thiosulfate, washed with brine, dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (80-g Redi-Sep Gold column, 0-15% Et20/Heptane) to afford 2,3-dichloro-5-iodo-6-methoxypyridine (6.29 g, 20.70 mmol, 76% yield) as a white solid. m/z (ESI) 304.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-b0b7adfc7d2341d09fd1d3e83f27cb44
Source noteuspto-grants-2015_12