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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423205Generated: October 29, 2026

Potassium Iodide → 5-Chloro-2-iodophenol

https://huagongshe.com/reaction/423205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-Amino-5-chlorophenolHCID 91591—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventHCID 86640070HCID 86640070—
Product5-Chloro-2-iodophenolHCID 661333379.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-5-chlorophenol (5.7 g, 40 mmol) is dissolved in DMSO/water/H2SO4 (200/60/140 mL) and cooled to 0° C. To this solution is added sodium nitrite (4.1 g, 60 mmol) in water (20 mL) and the mixture is stirred for 1 h at 0° C. To the mixture is added potassium iodide (19.9 g, 120 mmol) in water (20 mL) and the mixture is stirred at room temperature for 1 h. Another batch of potassium iodide (19.9 g, 120 mmol) in water (20 mL) is added and the mixture is stirred at room temperature for 1 h. The mixture is diluted with ethyl acetate, washed with water, saturated aqueous sodium sulfate, and brine. The organic portion is dried over MgSO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (Biotage™ Si65M, 20% ethyl acetate/hexane) to yield 8.09 g (79%) of the title compound as a pink solid. GCMS m/e 254 [M]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101760B2
Source datasetuspto-grants-2012_01
ORD IDord-02538b3ef1624a1cbf65babef0e1495f
Source noteuspto-grants-2012_01