HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559573Generated: October 29, 2026
8-Hydroxyquinoline → (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol
https://huagongshe.com/reaction/559573
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Diiodofluorobenzene | HCID 2737096 | — |
| Reactant | HCID 178418488 | HCID 178418488 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol | HCID 66974146 | — |
Reaction Steps
A mixture of 2,5-diiodofluorobenzene II-4 (2.50 g, 7.18 mmol), 4-hydroxymethylimidazole hydrochloride (0.967 g, 7.18 mmol), 8-hydroxyquinoline (0.104 g, 0.717 mmol) and K2CO3 (2.00 g, 14.5 mmol) in DMSO (12 mL) was degassed with Ar before being charged with CuI (0.136 g, 0.716 mmol). The mixture in a sealed tube was heated at 130° C. overnight. After being cooled to room temperature, H2O and EtOAc were added. It was filtered through celite. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was purified by a silica gel column, eluted with MeOH in CH2Cl2 (0-5% MeOH) to give (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol (0.39 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063077B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-644ea834527f40268b6482fe0ee57ea7 |
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| Source note | uspto-grants-2011_11 |
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