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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046022Generated: November 2, 2026

Iodine → 4-Hydroxy-3-iodobenzonitrile

https://huagongshe.com/reaction/2046022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-CyanophenolHCID 13019—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
Product4-Hydroxy-3-iodobenzonitrileHCID 1095581580.1%

Reaction Steps

To a solution of 4-hydroxybenzonitrile (0.5 g; 4.18 mmol) in 25% NH4OH (22 ml) a solution of I2 (1.06 g; 4.18 mmol) and KI (3.41 g; 20.54 mmol) in H2O (5 ml) was added at once with stirring. The stirring was continued for 6 h, during which time the mixture turn from black into colourless. The precipitate formed was filtered off and filtrate was evaporated to dryness under reduced pressure. The residue was treated with H2O (3 ml). The precipitate formed was filtered off, washed with cold H2O (3×2 ml), and dried in vacuo to give the title compound (0.82 g; 80%), as colourless solid. 1H-NMR (CDCl3) 7.96 (d, 1H, 1.9 Hz); 7.53 (dd, 1H, J=1.9 Hz, 8.5 Hz); 7.03 (d, 1H, J=8.5 Hz); 6.03 (s, 1H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592399B2
Source datasetuspto-grants-2013_11
ORD IDord-3e66a565a4e1482097f9ac81dd37c449
Source noteuspto-grants-2013_11