HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furancarboxaldehyde, tetrahydro- → HCID 86608736, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| Reactant | HCID 86608737 | HCID 86608737 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86608736 | HCID 86608736 | — |
Reaction Steps
To 5% palladium on carbon (0.05 g) under nitrogen was added a solution of 1,1-dimethylethyl-(3S)-3-aminopiperidine-1-carboxylate (0.50 g, 2.5 mmol) and tetrahydrofuran-3-carboxaldehyde (50% w/w in water) (0.50 g, 2.5 mmol) in ethanol (20 mL). The reaction mixture was hydrogenated overnight at 60 psi in a Parr hydrogenator. The catalyst was removed by filtration through Celite and the solvent removed in vacuo to give 1,1-dimethylethyl (3S)-3-[(tetrahydrofuran-3-ylmethyl)amino]piperidine-1-carboxylate as a colourless, slightly cloudy oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432280B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-38ead057f5fe4025b7206aaf17f56a70 |
| Source note | uspto-grants-2008_10 |