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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251123Generated: November 4, 2026

Sodium Iodide → 4-(6,7-dihydro-5H-1,4,8a-triaza-s-indacen-8-yl)-2-iodo-phenol

https://huagongshe.com/reaction/2251123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
ReactantSodium HypochloriteHCID 23665760—
Reactant4-(6,7-Dihydro-5H-1,4,8a-triaza-s-indacen-8-yl)-phenolHCID 136057243—
SolventMethanolHCID 887—
Product4-(6,7-dihydro-5H-1,4,8a-triaza-s-indacen-8-yl)-2-iodo-phenolHCID 136057242—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(6,7-Dihydro-5H-1,4,8a-triaza-s-indacen-8-yl)-phenol (500 mg, 0.002 mmol) was dissolved in methanol (10 mL) followed by addition of NaI (368 mg, 2.45 mmol) and NaOH (98 mg, 2.45 mmol). The solution was cooled to 0° C. followed by dropwise addition of NaOCl (5.25% aq, 3.8 ml) over 3 minutes. The reaction mixture was stirred at 0° C. for 1 hour followed by warming to room temperature and quenching with sodium thiosulphate (saturated. aq., 6 ml). The pH of the reaction was adjusted to ˜7 by addition of sodium dihydrogen phosphate. The solution was extracted with CH2Cl2. The organic layer was dried and concentrated. The residue was purified on silica gel (10%→60% EtOAc in hexane) to give 4-(6,7-dihydro-5H-1,4,8a-triaza-s-indacen-8-yl)-2-iodo-phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319103B2
Source datasetuspto-grants-2008_01
ORD IDord-39327a82a1a64bd882b580c972bcd673
Source noteuspto-grants-2008_01