Réaction #51410

Équation de réaction

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

Rendement 41.0%

Solvants

THF

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGthe reaction mixture was stirred overnight
2. 2
   Extractionthis mixture was extracted with ethyl acetate
3. 3
   Lavagethe organic extracts washed with water
4. 4
   Autredried
5. 5
   Concentrationconcentrated under reduced pressure
6. 6
   AutreThe residue was triturated with ether/hexanes
7. 7
   Autrethe solvents decanted
8. 8
   Autrethe residue dried under reduced pressure

Mode opératoire

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).

Source