تفاعل #51410

ord-e742757927f04d84bc0649873d9fadf1

معادلة التفاعل

Cl
HCl
CC(C)CCON=O
Isoamyl nitrite
O=C1CC2CCC(C2)C1Cc1ccccn1
2-aza-2-benzyl-3-oxobicyclo[3.2.1]octane
C1CCOC1.CC(C)(C)[O-].[K+]
t-BuOK THF
O=C1C(=NO)C2CCC(C2)C1Cc1ccccn1
2-aza-2-benzyl-4-oximino-3-oxobicyclo[3.2.1]octane
المردود 41.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe reaction mixture was stirred overnight
  2. 2
    استخلاصthis mixture was extracted with ethyl acetate
  3. 3
    غسيلthe organic extracts washed with water
  4. 4
    أخرىdried
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىThe residue was triturated with ether/hexanes
  7. 7
    أخرىthe solvents decanted
  8. 8
    أخرىthe residue dried under reduced pressure

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849650B2uspto-grants-2005_02