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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377813Generated: October 30, 2026

Potassium Iodide → 2-(2-tert-Butylphenoxy)-3-iodopyridine

https://huagongshe.com/reaction/2377813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium NitriteHCID 23668193—
Reactant2-(2-Tert-butylphenoxy)pyridin-3-amineHCID 28605427—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product2-(2-tert-Butylphenoxy)-3-iodopyridineHCID 5985743556%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium nitrite (157 mg, 2.28 mmol) in water (1 mL) was added to a mixture of 2-(2-tert-butylphenoxy)-3-aminopyridine (prepared above according to 1b) (500 mg, 2.07 mmol) in (1:1) conc. HCl: water (14 mL) at 0° C. The mixture was stirred at 0° C. for 15 min and a solution of potassium iodide (1.0 g, 6.22 mmol) in water (2 mL) was added. The mixture was stirred at 60° C. for 1.5 h and allowed to cool down to rt. A solution of sodium bisulfite was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried (anhydrous sodium sulfate), filtered and evaporated. The residue was purified by flash-chromatography (dichloromethane:hexanes/20:100) to afford 394 mg (56%) of 2-(2-tert-butylphenoxy)-3-iodopyridine. (M+H)+=354.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470712B2
Source datasetuspto-grants-2008_12
ORD IDord-8c9bbd5966a24a6e86aed3b3ccb78b3d
Source noteuspto-grants-2008_12