HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (E)-3-[4,5-Bis(4-fluorophenyl)-2-trifluoromethyl-1H-imidazol-1-yl]-2-propenenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dibromopropanenitrile | HCID 107299 | — |
| Reactant | 4,5-bis(4-fluorophenyl)-2-trifluoromethyl-1H-imidazole | HCID 14849768 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-3-[4,5-Bis(4-fluorophenyl)-2-trifluoromethyl-1H-imidazol-1-yl]-2-propenenitrile | HCID 14849771 | 41.1% |
Reaction Steps
From 4,5-bis(4-fluorophenyl)-2-trifluoromethyl-1H-imidazole (3.045 g), 2,3-dibromopropionitrile (5.33 g), anhydrous potassium carbonate (3.1 g) and triethylamine (5.2 ml) in dry DMF (19 ml) by the process as described for the preparation of Intermediate (3a) to afford a dark brown residue which was purified by FCC using gradient elution with System A (5-15% with 5% incremental increase of ethyl acetate per 500 ml eluant) to afford the title compound (1.449 g) as a white solid. νmax (CHBr3) 2229 cm-1 (C≡N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120848 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-a3f7ff7f0a674529aeca0dc30bfb080b |
| Source note | uspto-grants-1992_06 |