HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl morpholine oxide → 2-Benzyl-2-azabicyclo[2.2.2]octan-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | (6S)-2-Benzyl-2-azabicyclo[2.2.2]octan-6-OL | HCID 2802928 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Benzyl-2-azabicyclo[2.2.2]octan-6-one | HCID 12317473 | 81% |
Reaction Steps
To a vigorously stirring suspension of (6S)-N-benzyl-2-azabicyclo[2.2.2]octan-6-ol (1.5 g, 6.9 mmol, Maybridge) and activated 4 Å MS (1.0 g) in acetonitrile (70 mL) at 23° C. was sequentially added 4-methylmorpholine-N-oxide (1.2 g, 10 mmol) and tetrapropylammonium perruthenate (240 mg, 0.69 mmol). After stirring the resulting black suspension for 30 min, the mixture was concentrated in vacuo, and the resulting residue was purified by flash chromatography (20-50% ethyl acetate in hexanes) to provide N-benzyl-2-azabicyclo[2.2.2]octan-6-one as an orange oil (1.2 g, 81%). MS (AP CI) 216 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586446B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-36e8970fc345449f97b99de1ee05b1ab |
| Source note | uspto-grants-2003_07 |