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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 9-Methyl-3,9-diazabicyclo(4.2.1)nonan-4-one | HCID 557466 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-Methyl-3,9-diazabicyclo[4.2.1]nonane | HCID 13973730 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399457B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-1182d64edc7f4c0bab5e87d3d759b2fd |
|---|
| Source note | uspto-grants-2013_03 |
|---|