HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092185Generated: November 1, 2026
Imidazole → 4-((1H-imidazol-1-yl)methyl)-2-methylbenzonitrile
https://huagongshe.com/reaction/2092185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1001055-64-6 | HCID 22615981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((1H-imidazol-1-yl)methyl)-2-methylbenzonitrile | HCID 57517525 | 58% |
Reaction Steps
To the suspension of potassium carbonate (2.16 g, 15.7 mmol) in THF at room temperature was added imidazole (4.27 g, 62.8 mmol). The mixture was stirred at room temperature for 10 minutes then 4-(bromomethyl)-2-methylbenzonitrile (CAS 1001055-64-6) (6.6 g, 31.4 mmol) was added and refluxed for 24 hours. The mixture was then cooled to room temperature. Potassium carbonate was filtered off. The filtrate was concentrated and residue was redissolved in dichloromethane. The dichloromethane phase was washed with water (three times) and then HCl (three times). To the combined HCl phase was added sodium carbonate (solid) and extracted with ethyl acetate. Ethyl acetate phase was washed with water and brine, dried over sodium sulfate and concentrated. Column chromatography (10% methanol/ethyl acetate) gave 4-((1H-imidazol-1-yl)methyl)-2-methylbenzonitrile (3.59 g, 58%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440698B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-c0c4cfe101fb47f9bfb0e32ad6e1e3c3 |
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| Source note | uspto-grants-2013_05 |
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