반응 #3428

ord-5b22770333014a4da72ab520662759f7

반응 조건

온도
-30°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGto stir for 30 minutes at -30° C.
  2. 2
    온도to warm to room temperature
  3. 3
    workup.STIRRINGstir for 1 hour
  4. 4
    기타the phases were separated
  5. 5
    추출extracted with CH2Cl2 (2×)
  6. 6
    건조dried (MgSO4)
  7. 7
    농축concentrated
  8. 8
    기타the residue was chromatographed (silica gel; CHCl3 /MeOH, 95:5)

실험 절차

3-Bromo-3-phenylpyridine (200 mg, 0.85 mmol) was dissolved in Et2O and cooled to -30° C. A solution of 2.5M t-BuLi (1.1 mL, 1.90 mmol) in pentane was added, and the reaction was stirred for 10 minutes. 1,2,3,5,6,7-Hexahydropyrrolizinium perchlorate (230 mg, 1.30 mmol) was added, and the reaction mixture was allowed to stir for 30 minutes at -30° C. then allowed to warm to room temperature and stir for 1 hour. Then 2N HCl was added, the phases were separated, and the aqueous phase was basified with 15% NaOH and extracted with CH2Cl2 (2×). The organic phases were combined, dried (MgSO4) and concentrated, and the residue was chromatographed (silica gel; CHCl3 /MeOH, 95:5) to afford a clear oil (32.5 mg).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733912uspto-grants-1998_03