Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzimidazole | HCID 5798 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-3-(bromomethyl)-2-methylbenzene | HCID 22672648 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59375036 | HCID 59375036 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-fd68c981dc4a48aabfaf310968681ba2 |
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| Source note | uspto-grants-2013_01 |
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