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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 178433060HCID 178433060—
CatalystCopper TMEDAHCID 86657874—
SolventTetrahydrofuranHCID 8028—
Product4-iodo-2-methyl-1-phenyl-1H-imidazoleHCID 5751664840%
Product5-iodo-2-methyl-1-phenyl-1H-imidazoleHCID 5751664935%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518945B2
Source datasetuspto-grants-2013_08
ORD IDord-7da57c807df84a3fa07162b777d0698f
Source noteuspto-grants-2013_08