HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-(6-Nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine → 1-(2-(6-Aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-(6-Nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine | HCID 18986586 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(2-(6-Aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidine | HCID 22362101 | — |
Reaction Steps
A suspension of 3.2 g of 1-(2-(6-nitrotetralin-1-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine in 50 ml of methanol is hydrogenated in the presence of 1.6 g of Pd/C (5%) until the absorption of hydrogen has come to a standstill. The catalyst is filtered off, and the filtrate is worked up in the customary manner and gives 1-(2-(6-aminotetralin-1-yl) ethyl)-4-(3,4-dimethoxyphenyl)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05495022 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-635128aeb4064d568739f15449e11af7 |
| Source note | uspto-grants-1996_02 |