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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250479Generated: October 31, 2026

Toluene → HCID 59641868, compound

https://huagongshe.com/reaction/2250479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhenylboronic AcidHCID 66827—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
Reactant2,4,5-tribromo-1-[[2-(trimethylsilyl)ethoxy]methyl]-1H-ImidazoleHCID 10906203—
SolventSodium CarbonateHCID 10340—
ProductHCID 59641868HCID 5964186839%

Reaction Conditions

Temperature90 °C

Reaction Steps

Through a mixture of 2,4,5-tribromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole [Lipshutz et al. (Tet Lett 1992, 33, 5865-5868)] (3.75 g, 7.09 mmol) and phenyl boronic acid (865 mg, 7.09 mmol) in 2 M aqueous sodium carbonate (7.09 mL) and a 5:1 mixture of toluene:methanol (168 mL) was bubbled nitrogen gas for 10 min. Palladium tetrakis triphenylphosphine (820 mg, 0.71 mmol) was added to the mixture that was then heated under nitrogen at 90° C. for 2 h. To the reaction mixture was added 4-methoxy phenyl boronic acid (1.19 g, 7.80 mmol) and another 2 M aqueous sodium carbonate (7 mL). The mixture was refluxed 4 h. The mixture was then concentated in vacuo and purified by flash column chromatography (silica gel, 20% ethyl acetate in hexanes) to provide the title compound as an oil (1.26 g, 39% yield). MS m/e 461; HPLC retention time 4.31 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317032B2
Source datasetuspto-grants-2008_01
ORD IDord-117b03366f5649d0a8762a9b09351bfe
Source noteuspto-grants-2008_01