HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22126993, compound → HCID 22128196, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22126993 | HCID 22126993 | — |
| Catalyst | HCID 57448735 | HCID 57448735 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22128196 | HCID 22128196 | 79% |
Reaction Steps
A solution of 2.0 g (6.72 mmol) of (3RS,4RS)-l-benzyl-4-(4-hydroxymethyl-phenyl)-piperidin-3-ol in 100 ml of ethanol was hydrogenated at room temperature and 3 bar for 4 hours in the presence of 1.0 g of palladium oxide/charcoal (20%). For the working-up, the catalyst was filtered off under suction over Dicalit and the residue was washed twice with 50 ml of ethanol each time. The ethanol solution was evaporated under reduced pressure and the residue was chromatographed on silica gel using a 65:10:1 mixture of methylene chloride, methanol and ammonia as the eluent. There were obtained 1.1 g (79% of theory) of (3RS,4RS)-4-(4-hydroxymethyl-phenyl)-piperidin-3-ol as a colourless solid; MS: 207 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051712 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-ed0e638efccb46298adeca8cccc479f9 |
| Source note | uspto-grants-2000_04 |