Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393202Generated: October 31, 2026

9-Benzyl-3-oxa-9-azabicyclo(3.3.1)nonan-7-one → 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one

https://huagongshe.com/reaction/1393202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Benzyl-3-oxa-9-azabicyclo(3.3.1)nonan-7-oneHCID 15639114—
CatalystPalladiumHCID 23938—
SolventEthyl acetate acetateHCID 22609514—
Product3-Oxa-9-azabicyclo[3.3.1]nonan-7-oneHCID 55288333—

Reaction Steps

To a stirring mixture of 9-benzyl-3-oxa-9-aza-bicyclo[3.3.1]nonan-7-one (1.1 g, 4.76 mmol) in EtOAc/HOAc (6 mL, 1:1, v/v) was added palladium on carbon (250 mg). The resulting mixture was stirred at room temperature under an atmosphere of hydrogen for 2 days. The suspension was filtered through Celite and the filtrate was concentrated under vacuum to give a quantitative yield of 3-oxa-9-aza-bicyclo[3.3.1]nonan-7-one as a yellow oil. This crude mixture was converted to the corresponding hydrochloric salt by the addition of HCl (3 mL, 1N aqueous HCl). The mixture was concentrated under reduced pressure and this process was repeated twice. Retention time (min)=0.231, Method [1], MS(ESI) 142.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345056B2
Source datasetuspto-grants-2008_03
ORD IDord-170c5bf807f74809b9383a612f50339d
Source noteuspto-grants-2008_03