HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamine → 3-(4-Acetoxy-4-phenylpiperidin-1-yl)propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamine | HCID 22993462 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4-Acetoxy-4-phenylpiperidin-1-yl)propylamine | HCID 10778852 | 99.6% |
Reaction Steps
A mixture of N-benzyloxycarbonyl-3-(4-acetoxy-4-phenylpiperidin-1-yl)propylamine (3.0 g, 7.3 mmol) and 10% Pd-C (0.3 g) in 1M ammonia in methanol(50 mL) was hydrogenated at 70 psi at room temperature for 4 h. The catalyst was removed by filtration and the solvent was evaporated to leave the product as a viscous oil (2.01 g, 99%), the 1H-NMR showed it to be very pure and was used in the next step without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06159990 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-1662d06c2ece48718c3f2d02a5ba54b8 |
| Source note | uspto-grants-2000_12 |