HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051729Generated: October 31, 2026
Allyl bromide → 1-allyl-2-bromo-1H-benzo[d]imidazole
https://huagongshe.com/reaction/1051729
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Bromobenzimidazole | HCID 2776281 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-allyl-2-bromo-1H-benzo[d]imidazole | HCID 118076210 | 52% |
Reaction Steps
A mixture of 2-bromo-1H-benzo[d]imidazole (0.400 g, 2.04 mmol), allyl bromide (0.35 mL, 4.08 mmol), 1,4-dioxane (15 mL), and 2 M aqueous sodium hydroxide solution (15 mL, 3.00 mmol) stirred for 2 h at 100° C. The reaction mixture was cooled to room temperature and diluted with ethyl acetate (50 mL). The organic phase was separated and washed with brine (30 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified via preparative thin layer chromatography (eluting with 20% ethyl acetate/petroleum ether) to afford 1-allyl-2-bromo-1H-benzo[d]imidazole (0.251 g, 52%) as a yellow oil. MS (ESI, pos. ion) m/z 237, 239 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388161B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-7205731dc75748158df4228c83848a72 |
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| Source note | uspto-grants-2016_07 |
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