HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-(2-benzyloxyphenyl)-4-piperidinol → 4-(2-Hydroxyphenyl)piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-(2-benzyloxyphenyl)-4-piperidinol | HCID 11824889 | — |
| Catalyst | HCID 178420936 | HCID 178420936 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Hydroxyphenyl)piperidin-4-ol | HCID 11106219 | 108.3% |
Reaction Steps
In 100 mL of methanol was dissolved 12 g (32 mmol) of 1-benzyl-4-(2-benzyloxyphenyl)-4-piperidinol. To the resulting solution was added 3 g of 20% palladium hydroxide carbon and the resulting mixture was subjected to catalytic reduction at room temperature for 6 hours under 4 atmospheric pressure. After completion of the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure, whereby 6.7 g (yield: 100%) of 4-(2-hydroxyphenyl)-4-piperidinol was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362203B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-18c51b328e9a4df6b9aeb99cbe100b9f |
| Source note | uspto-grants-2002_03 |