HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 69064282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)benzyl bromide | HCID 2737578 | — |
| Reactant | tert-Butyl (3S)-3-[(propan-2-yl)amino]pyrrolidine-1-carboxylate | HCID 53346612 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69064282 | HCID 69064282 | — |
Reaction Steps
A solution of 1,1-dimethylethyl (3S)-3-[(1-methylethyl)amino]pyrrolidine-1-carboxylate (0.34 g, 1.5 mmol) and 2-(trifluoromethyl)-5-fluorobenzyl bromide (0.58 g, 2.25 mmol) in acetonitrile (5 mL) was heated at reflux with anhydrous potassium carbonate (0.41 g, 3 mmol) for 24 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with water. The organic extracts were washed with brine, dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (0:100 to 10:90), to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07619096B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-548bddb55514412eb9b58a507f2fe27a |
| Source note | uspto-grants-2009_11 |