Reaktion #51410

Reaktionsgleichung

HCl

Isoamyl nitrite

2-aza-2-benzyl-3-oxobicyclo[3.2.1]octane

t-BuOK THF

→

2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane

Ausbeute 41.0%

Lösungsmittel

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe reaction mixture was stirred overnight
2. 2
   Extraktionthis mixture was extracted with ethyl acetate
3. 3
   Waschenthe organic extracts washed with water
4. 4
   Sonstigedried
5. 5
   Einengenconcentrated under reduced pressure
6. 6
   SonstigeThe residue was triturated with ether/hexanes
7. 7
   Sonstigethe solvents decanted
8. 8
   Sonstigethe residue dried under reduced pressure

Vorschrift

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).

Quelle