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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478951Generated: October 26, 2026

3-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione → 3-Benzyl-3,8-diazabicyclo[3.2.1]octane

https://huagongshe.com/reaction/1478951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dioneHCID 14839575—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product3-Benzyl-3,8-diazabicyclo[3.2.1]octaneHCID 1243059452%

Reaction Steps

A solution of 3-benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione LXVI (0.00108 mol, 250 mg) in dry ether (2 mL) was added to a stirred suspension of LiAlH4 (122 mg, 0.00315 mol) in dry ether (8 mL) at 0° C. under nitrogen atmosphere. The reaction bath was allowed to return at room temperature and stirring was continued for 30 h. After completion of the reaction (checked by TLC), the reaction mixture was quenched with chilled water and then stirred for 1 h. The reaction mixture was diluted with ether (20 mL) and the organic layer was washed with water, dried over Na2SO4, concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 60-120 mesh; EA-Hexane, 1:1) to afford the product LXVII in 52% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09404081B2
Source datasetuspto-grants-2016_08
ORD IDord-ed50a00057fe4d4ba5e4125a6e736fcc
Source noteuspto-grants-2016_08