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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743702Generated: November 1, 2026

Water → 3-Benzyl-3,8-diazabicyclo[3.2.1]octane

https://huagongshe.com/reaction/1743702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-Benzyl-3,8-diazabicyclo[3.2.1]octane-2,4-dione hydrochlorideHCID 22235587—
SolventTetrahydrofuranHCID 8028—
Product3-Benzyl-3,8-diazabicyclo[3.2.1]octaneHCID 12430594101.3%

Reaction Steps

3-Benzyl-3,8-diazabicyclo[3.2.1]octan-2,4-dione (28 g, 0.10 mol; from step (d) above) was added in portions to a suspension of LiAlH4 (19 g, 0.50 mol) in THF (500 mL). After addition of the solid, the reaction was slowly warmed to reflux, and then refluxed overnight. The reaction was cooled in an ice bath. To the cold reaction mixture there was added sequentially H2O (19 mL), 15% NaOH solution (19 mL) and H2O (57 mL). The resulting mixture was stirred for 30 min then filtered through a pad of Celite®. The filtrate was concentrated in vacuo to afford 20.5 g (86%) of the sub-title compound as a golden oil. A hydrochloride salt may be obtained from CH3CN and a solution of hydrogen chloride in EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012074B2
Source datasetuspto-grants-2006_03
ORD IDord-3ddc5af7a94e447c9ad0e8ba0f011246
Source noteuspto-grants-2006_03