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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84157Generated: October 29, 2026

9-((Z)-cyclooct-2-enyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-one → 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one, 9-cyclooctyl-

https://huagongshe.com/reaction/84157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-((Z)-cyclooct-2-enyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-oneHCID 59451300—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Oxa-9-azabicyclo[3.3.1]nonan-7-one, 9-cyclooctyl-HCID 59451137—

Reaction Conditions

Temperature25 °C

Reaction Steps

In a manner similar to Example 32, the compound of formula MG, 9-((Z)-cyclooct-2-enyl)-3-oxa-9-azabicyclo[3.3.1]nonan-7-one, was prepared from the compound of formula MF except that the compound of formula ME was used in place of the compound of formula JC (yield 90%). Under a hydrogen atmosphere, a mixture of the compound of formula MG, 5% palladium on carbon (1.0 g, Sigma-Aldrich), and EtOH (20 mL) was stirred at a temperature of about 25° C. for 4 h. After the Pd/C was filtered off, the filtrate was concentrated under reduced pressure to provide the compound of formula MH, 9-cyclooctyl-3-oxa-9-azabicyclo[3.3.1]nonan-7-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846929B2
Source datasetuspto-grants-2014_09
ORD IDord-75a1a2b77b0046ca8480a7bc0a18d96a
Source noteuspto-grants-2014_09