HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898629Generated: November 2, 2026
Phenylboronic Acid → 4-iodo-2-methyl-1-phenyl-1H-imidazole
https://huagongshe.com/reaction/1898629
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 178433060 | HCID 178433060 | — |
| Catalyst | Copper TMEDA | HCID 86657874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-iodo-2-methyl-1-phenyl-1H-imidazole | HCID 57516648 | 40% |
| Product | 5-iodo-2-methyl-1-phenyl-1H-imidazole | HCID 57516649 | 35% |
Reaction Steps
4-Iodo-2-methyl-1H-imidazole (1.0 g, 4.8 mmol) was dissolved in 30 mL of THF. Copper TMEDA catalyst (447 mg, 0.96 mmol, Aldrich) and then phenylboronic acid (0.41 g, 3.35 mmol) were added. Oxygen gas was bubbled into the reaction mixture for 20 min, then the mixture was stirred at room temperature for 90 min. An additional 0.21 g of phenylboronic acid was added followed by an additional 20 min of oxygen gas bubbling and 75 min of stirring at room temperature. An additional 0.21 g of phenylboronic acid was added followed by an additional 20 min of oxygen gas bubbling and then stirring at room temperature for 20 h. The reaction mixture was filtered through a bed of neutral alumina, concentrated and purified by silica gel chromatography (ethyl acetate/hexanes) to give 0.55 g (40%) of 4-iodo-2-methyl-1-phenyl-1H-imidazole ((M+H)+=285) and 0.47 g (35%) of 5-iodo-2-methyl-1-phenyl-1H-imidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518945B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-7da57c807df84a3fa07162b777d0698f |
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| Source note | uspto-grants-2013_08 |
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