HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441203Generated: November 2, 2026
Imidazole → 1,3-bis((1H-imidazol-1-yl)methyl)benzene
https://huagongshe.com/reaction/1441203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, 1,3-bis(bromomethyl)- | HCID 69373 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3-bis((1H-imidazol-1-yl)methyl)benzene | HCID 11228701 | 63.9% |
Reaction Steps
To a 500 mL round bottom flask equipped with a stirbar was added 11.6 g imidazole (170 mmol) and 9.55 g (170 mmol) finely pulverized potassium hydroxide. These were stirred in 200 mL acetone until the solution became yellow translucent. 15.0 g (56.8 mmol) α,α′-dibromo-m-xylene was then added, and the solution was stirred at room temperature overnight. The cloudy solution was filtered, and the white solids rinsed with acetone. The resulting filtrate was dried on silica and partitioned on a silica gel column using 30/70 acetonitrile/methanol as eluent. The product fractions were evaporated of solvent and the resulting oil recrystallized from ethyl acetate/hexanes to give 8.65 g 1-[3-(1H-imidazole-1yl-methyl)benzyl]-1H-imidazole as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07655322B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-c080b0cb6fe949c8a7c8a5bbb2ee371b |
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| Source note | uspto-grants-2010_02 |
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