HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13192226, compound → HCID 13192228, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13192226 | HCID 13192226 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13192228 | HCID 13192228 | — |
Reaction Steps
16.0 g (0.04 mol) of trans-3-acetoxy-4-(3,4-dimethyl-phenoxy)-1-carbobenzyloxy-piperidine are dissolved in 400 ml of methanol and hydrogenated in the presence of 1.5 g of a 5% strength palladium-on-charcoal catalyst under normal pressure. After the reaction has ended, the catalyst is filtered off by means of a layer of diatomaceous earth and the filtrate is evaporated under a water pump vacuum, whereupon trans-3-acetoxy-4-(3,4-dimethylphenoxy)-piperidine is obtained in the form of a yellow oil. Reaction of the base with fumaric acid in ethanol/ether gives the crystalline acid fumarate with a melting point of 170°-172°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04160837 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-eb1d45ae8a8a4bbe8e85dbb7e8fca1cd |
| Source note | uspto-grants-1979_07 |