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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752044Generated: October 28, 2026

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

https://huagongshe.com/reaction/1752044

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 (1′, 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 numberUS09162988B2
Source datasetuspto-grants-2015_10
ORD IDord-a12596d4f3fe456782d238d9a882f497
Source noteuspto-grants-2015_10