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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873153Generated: October 30, 2026

2-Hydroxybenzonitrile → 2-Hydroxy-5-iodo-benzonitrile

https://huagongshe.com/reaction/873153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-HydroxybenzonitrileHCID 11907—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantN-IodosuccinimideHCID 120273—
SolventAcetonitrileHCID 6342—
Product2-Hydroxy-5-iodo-benzonitrileHCID 702304081,626.898%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-hydroxy-benzonitrile (47.6 g, 0.400 mmol) in CH3CN (500 mL) was added CF3SO3H (40 mL) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 20 min, and then NIS (108 g, 0.48 mmol) was added. The mixture was stirred at room temperature overnight, then concentrated, diluted with H2O (300 mL) and extracted with EA (300 mL×3). Combined organic portions were dried over sodium sulfate, filtered and reconcentrated. Purification via column chromatography on silica gel (petroleum ether/ethyl acetate=5/1) afforded the title product (80 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975400B2
Source datasetuspto-grants-2015_03
ORD IDord-208cf829163a47fbb7e5f1681ca406b2
Source noteuspto-grants-2015_03