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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685399Generated: November 4, 2026

Iodine → HCID 67292422, compound

https://huagongshe.com/reaction/1685399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant1,4-DibromobenzeneHCID 7804—
ReactantSodium HydroxideHCID 14798—
Reactant3-Hydroxypyridine-2-carbonitrileHCID 101920—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67292422HCID 6729242235%

Reaction Conditions

Temperature10 °C

Reaction Steps

48.5 g (205.5 mM) of 1,4-dibromobenzene are added dropwise to a mixture containing one crystal of iodine and 5 g (205.5 mM) of magnesium metal covered with 150 ml of THF. The mixture is stirred at the reflux temperature of the solvent for 2 hours and then cooled to 10° C. 12.34 g (102.7 mM) of 2-cyano-3-pyridinol are then added dropwise. The reaction medium is heated at the reflux temperature of the solvent for 3 hours, then stirred for 18 h at room temperature and then treated with 300 ml of 0.5 N sulfuric acid. The solvents are driven off under reduced pressure and the residual aqueous phase is brought to pH 4 by adding a necessary and sufficient amount of 2 N sodium hydroxide solution. The neutralized mixture is extracted with dichloromethane and the organic phase is dried over magnesium sulfate. After evaporation of the solvent, the expected product is obtained in the form of a yellow solid with a yield of 35%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148407B2
Source datasetuspto-grants-2012_04
ORD IDord-5138f20beedf431b96a033989ffd5101
Source noteuspto-grants-2012_04