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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946853Generated: October 26, 2026

Water → 9-Methyl-3,9-diazabicyclo[4.2.1]nonane

https://huagongshe.com/reaction/1946853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant9-Methyl-3,9-diazabicyclo(4.2.1)nonan-4-oneHCID 557466—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product9-Methyl-3,9-diazabicyclo[4.2.1]nonaneHCID 1397373069%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of LiAlH4 (0.61 g) in anhydrous THF (30 ml), cooled at 0° C., and kept under an argon inert atmosphere, a solution in THF of 9-methyl-3,9-diazabicyclo[4.2.1]nonan-4-one obtained in example 1 is dropwise added (1.00: of compound in 10 ml of THF). The obtained mixture is heated at reflux for 48 hours and then cooled at 0° C. Then water (3 ml) is slowly added to the mixture. After water addition, the mixture is kept under stirring for 1:0 minutes. A precipitate is formed, that at the end is filtered under vacuum and washed with dichloromethane. The obtained filtrate is evaporated obtaining an oil which is dissolved in dichloromethane. The obtained solution is then anhydrified on sodium sulphate and the solvent evaporated. The residual oil is distilled (45-50° C./0.1 mmHg) to give 0.63 g of 9-methyl-3,9-diazabicyclo[4.2.1]nonane (2a) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399457B2
Source datasetuspto-grants-2013_03
ORD IDord-1182d64edc7f4c0bab5e87d3d759b2fd
Source noteuspto-grants-2013_03