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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504476Generated: October 30, 2026

Iodine → HCID 117737295, compound

https://huagongshe.com/reaction/1504476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-Bromo-4-methoxybenzonitrileHCID 11218092—
CatalystSilver(I) trifluoromethanesulfonateHCID 76223—
SolventDichloromethaneHCID 6344—
ProductHCID 117737295HCID 11773729557.1%

Reaction Steps

A RBF was charged with 2-bromo-4-methoxybenzonitrile (891 mg, 4.20 mmol, Matrix Scientific) and DCM (1.68E+04 μl) to give a clear solution. silver trifluoromethanesulfonate (1188 mg, 4.62 mmol) and iodine (1173 mg, 4.62 mmol) were added in sequence. The resulting mixture was stirred for 2 d. Additional portions of silver trifluoromethanesulfonate (1188 mg, 4.62 mmol) and iodine (1173 mg, 4.62 mmol) were added, and the mixture was stirred for another 5 h. The reaction mixture was then filtered through celite with the aid of DCM. The filtrate was shaken with saturated aq. sodium thiosulfate until the color disappeared. The biphasic mixture was diluted with water then the layers were separated. The aq. layer was extracted with DCM (2×). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated. The residue was purified by chromatography on silica gel (40-g Redi-Sep Gold column, 25-g silica gel column, 5-30% EtOAc/Heptane) give 2-bromo-5-iodo-4-methoxybenzonitrile (811 mg, 2.400 mmol, 57.1% yield) as an off-white solid. m/z (ESI) 337.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-66ddfa6b86264cc7aee5e9f765e29dbf
Source noteuspto-grants-2015_12