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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360034Generated: October 31, 2026

4-Iodophenol → 2-(4-Iodophenoxy)pyrimidine

https://huagongshe.com/reaction/1360034

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChloropyrimidineHCID 74404—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product2-(4-Iodophenoxy)pyrimidineHCID 148461797.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

Under an argon atmosphere, potassium carbonate (207 mg) was added to a solution of 4-iodophenol (220 mg) and 2-chloropyrimidine (114 mg) in DMF (1 ml), and the resulting mixture was stirred at 120° C. for 3 hours. The reaction solution was cooled to room temperature and saturated brine was added thereto, followed by extracting the resulting mixture with chloroform. Organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent:hexane/ethyl acetate=3/1) to obtain 2-(4-iodophenoxy)pyrimidine (288 mg). NMR (H1, CDCl3): δ 6.97-7.00 (2H, m), 7.06 (1H, t, J=4.6 Hz), 7.73-7.75 (2H, m), 8.57 (2H, d, J=4.6 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879837B2
Source datasetuspto-grants-2011_02
ORD IDord-0a084a1546764f80bbea3920f84bf60b
Source noteuspto-grants-2011_02