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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602124Generated: October 29, 2026

1-(Benzyloxycarbonyl)-3-(tert-butyldimethylsilyloxymethyl)piperidine → Tert-butyl-dimethyl-(3-piperidylmethoxy)silane

https://huagongshe.com/reaction/602124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Benzyloxycarbonyl)-3-(tert-butyldimethylsilyloxymethyl)piperidineHCID 58992631—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl-dimethyl-(3-piperidylmethoxy)silaneHCID 5899262296%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902367B2
Source datasetuspto-grants-2011_03
ORD IDord-0b0a62a655e34190b0f76ee0e67e51cb
Source noteuspto-grants-2011_03