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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494757Generated: October 25, 2026

Sodium Iodide → 4-(4-Hydroxy-3-iodophenyl)benzonitrile

https://huagongshe.com/reaction/494757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
Reactant4'-Hydroxy-4-biphenylcarbonitrileHCID 140610—
ReactantSodium HypochloriteHCID 23665760—
ReactantMonosodium phosphateHCID 23672064—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventSodium ThiosulfateHCID 24477—
Product4-(4-Hydroxy-3-iodophenyl)benzonitrileHCID 1035867653%

Reaction Steps

To a solution of 4-hydroxy-4′-cyanobiphenyl (6.00 g, 30.8 mmol), sodium iodide (4.61 g, 30.8 mmol) and sodium hydroxide (1.23 g, 30.8 mmol) in methanol (90 mL) at 0° C. was added an aqueous solution of sodium hypochlorite (47 mL of 5.25% Clorox™, 2.29 g, 30.8 mmol) over 45 minutes. The mixture was stirred cold for 1 hour, warmed to ambient temperature and diluted with sodium thiosulfate solution (10 mL), water (80 mL) and adjusted to a pH of 7 by addition of sodium dihydrogen phosphate. The mixture was extracted with dichloromethane (2×90 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated under reduced pressure to give a white powder. The solid was crystallized from dichloroethane/hexane and chromatographed on silica with dichloromethane to give the titled compound (5.19 g, 53%). MS (DCI) m/z 339 [M+NH4+]+;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538138B2
Source datasetuspto-grants-2009_05
ORD IDord-10afbe2a3c434be99fcfd5926f3b75c8
Source noteuspto-grants-2009_05