HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylate | HCID 67067055 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 3-Pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate | HCID 67067076 | 83.5% |
Reaction Steps
10% Palladium-carbon (catalytic amount) was added to a THF (75 ml)/2-propanol (75 ml) solution containing 3-pyridyl 4-[4-(benzyloxy)phenoxy]-1-piperidinecarboxylate (3.7 g), and in a hydrogen gas atmosphere, this was stirred at room temperature under normal pressure for 24 hours. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure, and the resulting solid was washed with EtOAc/hexane, and dried under reduced pressure to obtain 3-pyridyl 4-(4-hydroxyphenoxy)-1-piperidinecarboxylate (2.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915261B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-e2cd58920407428aa5a96140fd0c0a5f |
| Source note | uspto-grants-2011_03 |