HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzyloxycarbonyl)-3-(tert-butyldimethylsilyloxymethyl)piperidine → Tert-butyl-dimethyl-(3-piperidylmethoxy)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzyloxycarbonyl)-3-(tert-butyldimethylsilyloxymethyl)piperidine | HCID 58992631 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl-dimethyl-(3-piperidylmethoxy)silane | HCID 58992622 | 96% |
Reaction Steps
10% palladium on activated carbon (1.32 g) was added to 1-(benzyloxycarbonyl)-3-(tert-butyldimethylsilyloxymethyl)piperidine (13.2 g, 36.3 mmol) in methanol (130 mL). The mixture was stirred at room temperature for 1 hour in a hydrogen atmosphere. Subsequently, the mixture was filtered through Celite, followed by evaporation of the solvent to give 7.96 g (96%) of the desired compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902367B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-0b0a62a655e34190b0f76ee0e67e51cb |
| Source note | uspto-grants-2011_03 |