HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl piperidin-4-ylmethoxyacetate, acetate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | ethyl N-(benzyloxycarbonyl)piperidin-4-ylmethoxyacetate | HCID 23370014 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl piperidin-4-ylmethoxyacetate, acetate salt | HCID 131719663 | 201.7% |
Reaction Steps
In a similar manner to Example 2, starting material step (c), the product from step (a) (1.4 g), ethanol (100 ml), glacial acetic acid (0.25 g), 10% Pd on C (140 mg) and hydrogen gas were reacted to give ethyl piperidin-4-ylmethoxyacetate, acetate salt (1.1 g), as a brown oil: NMR Spectrum (DMSO-d6) 1.12 (2H, m), 1.20 (3H, t), 1.62 (3H, m), 1.84 (3H, s), 2.48 (2H, m), 2.96 (2H, m), 3.29 (2H, d), 4.05 (2H, s), 4.12 (2H, q).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576334 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-4dcabb2e782742ecb0763e688d7c6d3d |
| Source note | uspto-grants-1996_11 |