HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Fluoroacetophenone → Ethanone, 1-[4-(4-ethyl-1H-imidazol-1-yl)phenyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178437183 | HCID 178437183 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethanone, 1-[4-(4-ethyl-1H-imidazol-1-yl)phenyl]- | HCID 45095120 | — |
Reaction Steps
NaH (0.068 g in 60% oil dispersion, 1.7 mmol) was added to a solution of compound 16 (0.180 g, 1.8 mmol) in DMF (6 mL) with stirring at room temperature. The mixture was stirred for 15 min and a solution of 4′-fluoroacetophenone (0.215 g, 1.56 mmol) in DMF (2 mL) was added. The reaction mixture was heated at 80° C. for 1 h, and then cooled, diluted with water, and extracted with EtOAc. The organic layer was washed with brine, dried, and evaporated to a yellow solid. Compound 17 crystallized to form white color needles upon standing at room temperature. The yield was 0.270 g, 67%. The structure was confirmed by 1H NMR in CDCl3. LC-MS: [M+1]=215. Purity was >98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017629B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-a2d57e49f5c44b90a2d91fafadd99227 |
| Source note | uspto-grants-2011_09 |