HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Mofegiline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | (E)-1-chloro-2-(fluoromethylene)-4-(p-fluorophenyl)butane | HCID 9815806 | — |
| Reactant | Sodium Diformylamide | HCID 10877056 | — |
| Solvent | Water | HCID 962 | — |
| Product | Mofegiline | HCID 6437850 | — |
Reaction Steps
Combine sodium diformylamide (28.8 g, 0.31 mol), acetonitrile (360 g), and N,N-dimethylformamide (48 g). Add (E)-1-chloro-2-(fluoromethylene)-4-(p-fluorophenyl)butane (50.6 g, 0.23 mol). Heat to reflux. After 5 hours, cool to ambient temperature. Add water (466 g) and stir for 15 minutes. After 30 minutes, the aqueous layer is removed. Evaporate the organic layer in vacuo to give the title compound. 1H NMR (CDCl3, 300 MHz) δ2.28 (m, 2H), 2.72 (m, 2H), 4.07 (d , J=3Hz, 2H), 6.74 (d, J=81Hz, 1H), 6.94 (m, 2H), 7.13 (m, 2H), 8.73 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05488188 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-850b8048dd1247e5be6b8ae2bcd7c948 |
| Source note | uspto-grants-1996_01 |