HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentane → 3-(Phenyl(4-(trifluoromethyl)phenyl)methyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | 3-(Phenyl(4-(trifluoromethyl)phenyl)methylene)piperidine | HCID 68734584 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Phenyl(4-(trifluoromethyl)phenyl)methyl)piperidine | HCID 68734510 | 99.4% |
Reaction Steps
To a solution of 3-(phenyl(4-(trifluoromethyl)phenyl)methylene)piperidine (1.0 g, 3.15 mmol) in methanol (25 mL) was charged with Pd/C under nitrogen atmosphere and fitted with hydrogen balloon using stopcock and covered with Teflon. The reaction mixture was stirred under hydrogen atmosphere for 8 h. It was filtered through celite, the celite was washed with methanol, and the solvent was removed under reduced pressure to afford the crude product which was then crashed out of pentane to give pure 3-(phenyl(4-(trifluoromethyl)phenyl)-methyl)piperidine (1.0 g, 98% yield) as a grey oil. MS (ESI, pos. ion) m/z: 320 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258306B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-711f1e37505e41bda5207720d6ccd7d1 |
| Source note | uspto-grants-2012_09 |