HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 4-(3-ethoxy-3-oxoprop-1-YN-1-YL)-4-hydroxypiperidine-1-carboxylate → tert-Butyl 4-(3-ethoxy-3-oxopropyl)-4-hydroxypiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 4-(3-ethoxy-3-oxoprop-1-YN-1-YL)-4-hydroxypiperidine-1-carboxylate | HCID 21955240 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | tert-Butyl 4-(3-ethoxy-3-oxopropyl)-4-hydroxypiperidine-1-carboxylate | HCID 21955349 | — |
Reaction Steps
Palladium on carbon (5%, 1 g) in water (10 mL) was added to a solution of 1,1-dimethylethyl 4-(3-ethoxy-3-oxo-1-propynyl)-4-hydroxy-1-piperidinecarboxylate (Description 76, 14.6 g, 0.046 mol) in ethanol (200 mL) and the mixture was shaken under hydrogen (45 psi) for 90 minutes. The mixture was filtered through a glass fibre pad and the solvent was evaporated under reduced pressure to give the title compound. m/z (ES+) 302 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105507B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-5d5e741348a8450b8a94e4bec562e9c6 |
| Source note | uspto-grants-2006_09 |