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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811048Generated: November 1, 2026

Benzimidazole → HCID 59375036, compound

https://huagongshe.com/reaction/1811048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3-(bromomethyl)-2-methylbenzeneHCID 22672648—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 59375036HCID 5937503682%

Reaction Steps

A mixture of 1-bromo-3-(bromomethyl)-2-methylbenzene (250 mg, 0.947 mmol), 1H-benzo[d]imidazole (336 mg, 2.84 mmol) and potassium carbonate (131 mg, 0.947 mmol) in acetonitrile (5 mL) was stirred at rt for 5 h, The mixture was diluted with EtOAc and filtered, and the solid was washed with EtOAc. The filtrate was washed with water, dried and concentrated. The residue was purified by column chromatography (eluting with a gradient from 60:40 hexane-EtOAc to EtOAc). to provide 1-(3-bromo-2-methylbenzyl)-1H-benzo[d]imidazole as a white solid (233 mg, 82%). 1H NMR (400 MHz, chloroform-d) δ 8.14 (1 H, s), 7.68-7.78 (1 H, m), 7.56 (1 H, d, J=7.9 Hz), 7.36-7.44 (1 H, m), 7.25-7.34 (2 H, m), 7.03 (1 H, t, J=7.8 Hz), 6.82 (1 H, d, J=7.7 Hz), 5.58 (2 H, s), 2.45 (3 H, s). Mass spectrum m/z 301, 303 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-fd68c981dc4a48aabfaf310968681ba2
Source noteuspto-grants-2013_01