HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230294Generated: October 25, 2026
4-Iodophenol → 2-(4-Iodophenoxy)pyrimidine
https://huagongshe.com/reaction/230294
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Iodophenol | HCID 10894 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(4-Iodophenoxy)pyrimidine | HCID 1484617 | 97.1% |
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 (HL, 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566724B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-5d89f388fe2c4c31b3e283302bee753a |
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| Source note | uspto-grants-2009_07 |
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