HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19029125, compound → 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19029125 | HCID 19029125 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine | HCID 19029146 | 981.2% |
Reaction Steps
A solution of 1-benzyloxycarbonyl-4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine (0.18 g) in ethanol (5 mL) was hydrogenated over 10% palladium on carbon (0.050 g) at a hydrogen pressure of 1 bar for 2 hours. The catalyst was then removed by filtration through diatomaceous earth, the filter cake was washed with ethanol and the solvent evaporated to afford the piperidine as a white crystalline solid (0.98 g); mp 64°-66° C.; NMR (CDCl3): 3.17 (m, 2), 2.98 (m, 1), 2.75 (dr,2, J=2.6, 12.0), 2.51 (s, 3), 2.01 (m, 2), 1.75 (m, 2); MS: m/z=196(M+1+28).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05654299 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-e6ce7915afab43cda9ddd22c7cd62fd1 |
| Source note | uspto-grants-1997_08 |