HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099451Generated: October 29, 2026
2-Methylimidazole → 3-(2-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)-benzonitrile
https://huagongshe.com/reaction/2099451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | 3-Fluoro-5-(trifluoromethyl)benzonitrile | HCID 519037 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-(2-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)-benzonitrile | HCID 67214643 | — |
Reaction Steps
A mixture of 3-fluoro-5-(trifluoromethyl)-benzonitrile (Lancaster Synthesis GmbH; 17 g, 89 mmol) and 2-methylimidazole (Fluka, Buchs, Switzerland; 22.2 g, 270 mmol) in N,N-dimethylacetamide (80 mL) is stirred at 145° C. for 19 h. The solvent is evaporated off under reduced pressure and the residue is dissolved in ethyl acetate (200 mL). The solution is washed with brine (200 mL), dried (Na2SO4) and the solvent is evaporated off under reduced pressure to give the crude product which is purified by recrystallisation from ether—hexane to afford the title compound as yellow crystalline solid, m.p. 132-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569566B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-319d93f8cd3548c0b4a89973d4b1207b |
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| Source note | uspto-grants-2009_08 |
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