HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylate → Ethyl 4-(2-aminoethyl)-1-benzyl-3-hydroxypiperidine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylate | HCID 86709485 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | Ethyl 4-(2-aminoethyl)-1-benzyl-3-hydroxypiperidine-4-carboxylate | HCID 86709519 | — |
Reaction Steps
Into a 10000-mL 4-necked round-bottom flask was placed a solution of ethyl 1-benzyl-4-(cyanomethyl)-3-oxopiperidine-4-carboxylate (180 g, 599.30 mmol) in acetic acid/methanol (1:1, 5.4 L) and platinum oxide (27 g, 118.90 mmol). The flask was then flushed and charged with hydrogen and stirred overnight at room temperature. After filtration under nitrogen through CELITE®, the filtrate was concentrated under vacuum to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206198B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-4582b30168db4c229d4ef8e76ec32a45 |
| Source note | uspto-grants-2015_12 |