HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Aza-2-benzyl-4-oximino-3-oxo-bicyclo[3,2,1]octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 2-Aza-2-benzyl-3-oxo-bicyclo[3,2,1]octane | HCID 22312669 | — |
| Reactant | KOtBu THF | HCID 66863523 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Aza-2-benzyl-4-oximino-3-oxo-bicyclo[3,2,1]octane | HCID 86584968 | 41% |
Reaction Steps
To a solution of 2-aza-2-benzyl-3-oxobicyclo[3.2.1]octane in THF was added 2.5 eq. of 1M t-BuOK/THF (Aldrich) and the resulting mixture was stirred for 30 minutes. Isoamyl nitrite (1.5 eq.) was then added dropwise and the reaction mixture was stirred overnight. To the reaction mixture was added 3N HCl and this mixture was extracted with ethyl acetate and the organic extracts washed with water, dried, and concentrated under reduced pressure. The residue was triturated with ether/hexanes, the solvents decanted and the residue dried under reduced pressure to afford 2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane as a tan liquid (41% yield). This procedure is further described in Y. Kim, Tetrahedron Lett. 30(21), 2833-2636 (1989).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559141B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-9a29c0e3faf34320a7c3d3431925280c |
| Source note | uspto-grants-2003_05 |