HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenethylamine → 1-(2-(1-Phenylethylamino)-4-fluorophenyl)-2,2,2-trifluoroethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenethylamine | HCID 7408 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2,4-Difluorophenyl)-2,2,2-trifluoroethanone | HCID 24726837 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2-(1-Phenylethylamino)-4-fluorophenyl)-2,2,2-trifluoroethanone | HCID 58707276 | 12% |
Reaction Steps
2,2,2-Trifluoro-1-(2,4-difluorophenyl)ethanone (1.59 g, 7.57 mmol), 1-phenylethanamine (0.92 g, 7.57 mmol) and N,N-diisopropylethylamine (1.95 g, 15.1 mmol) were stirred at room temperature in dry acetonitrile (50 mL) for 20 h. The solvent was evaporated and the residue was dissolved in dichloromethane and washed with water. The dichloromethane was evaporated and purified by silica chromatography in 20% ethyl acetate in hexanes to collect the title compound (0.28 mg, 12% yield). 1H NMR (400 MHz, CDCl3): δ 9.32 (s, 1H), 7.80 (t, 1H), 7.31 (m, 5H), 6.33 (t, 1H), 6.22 (d, 1H), 4.58 (m, 1H), 1.62 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968538B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-b6df97f825f24d7999b35083a03c85bc |
| Source note | uspto-grants-2011_06 |