HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl piperidin-4-yloxyacetate, acetate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl 1-benzyloxycarbonylpiperidine-4-oxyacetate | HCID 23370004 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl piperidin-4-yloxyacetate, acetate salt | HCID 131719662 | 192.1% |
Reaction Steps
In a similar manner to Example 2, starting material step (c), the product from step (a) (2.3 g), ethanol (200 ml), glacial acetic acid (0.6 ml), 10% Pd on C (200 mg) and hydrogen gas were reacted to give ethyl piperidin-4-yloxyacetate, acetate salt (1.7 g), as a brown oil: NMR Spectrum (DMSO-d6) 1.20 (3H, t), 1.41 (2H, m), 1.82 (3H, s), 1.86 (2H, m), 2.58 (2H, m), 2.95 (2H, m), 3.46 (1H, m), 4.11 (4H, m); Mass Spectrum m/Z 188 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576334 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-906650c6cd6d4607bdc27dfe139ecf45 |
| Source note | uspto-grants-1996_11 |