HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131714328, compound → HCID 131714327, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131714328 | HCID 131714328 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131714327 | HCID 131714327 | — |
Reaction Steps
Trans-1-benzyl-3-t-butyldimethylsilyloxy-4-(1-triphenylmethoxyprop-2-yl)piperidine (4.5 g; diastereomer A) was hydrogenated in ethanol (60 cm3) at 60° and 60 p.s.i. pressure over 10% palladium on carbon (0.9 g) for 5 hours. The solution was cooled, filtered through "Avicel" to remove the catalyst and evaporated in vacuo to afford trans-3-t-butyldimethylsilyloxy-4-(1-hydroxyprop-2-yl)piperidine as a crude oil (diastereomer A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04542132 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-b6b9317ff0c449bb90bb0b0e453db3a6 |
| Source note | uspto-grants-1985_09 |