Reacción #51410

Ecuación de reacción

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

Rendimiento 41.0%

Disolventes

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGthe reaction mixture was stirred overnight
2. 2
   Extracciónthis mixture was extracted with ethyl acetate
3. 3
   Lavadothe organic extracts washed with water
4. 4
   Otrodried
5. 5
   Concentraciónconcentrated under reduced pressure
6. 6
   OtroThe residue was triturated with ether/hexanes
7. 7
   Otrothe solvents decanted
8. 8
   Otrothe residue dried under reduced pressure

Procedimiento

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).

Fuente