HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Diazabicyclo(3.2.2)nonan-3-one → 1,4-Diazabicyclo(3.2.2)nonane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Diazabicyclo(3.2.2)nonan-3-one | HCID 4401850 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,4-Diazabicyclo(3.2.2)nonane | HCID 398407 | 90.2% |
Reaction Steps
To a stirred solution of 1,4-diazabicyclo[3.2.2]nonan-3-one (1.0 g, 7.2 mmol) in 1,4-dioxane (7.2 mL) at room temperature was added lithium aluminum hydride [2.0M/THF] (4.1 mL, 8.2 mmol). The reaction mixture was then heated at reflux for 6 hours before cooling to room temperature. The reaction was quenched by the stepwise addition of 200 □L of H2O, 200 □L of 15% aqueous NaOH, and 600 □L of H2O. The mixture was filtered through Celite which was subsequently washed with EtOAc. The combined filtrate was concentrated in vacuo to afford the product (0.82 g, 90%) which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 3.28-3.25 (m, 1H), 2.99-2.95 (m, 8H), 1.86-1.80 (m, 3H), 1.69-1.64 (m, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09139580B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-f0c770b3f612429bb01aec0ca7c7f95d |
| Source note | uspto-grants-2015_09 |