반응 #3425

ord-25cc9381e06f48dab75a6ffa0b61c21d

반응 조건

온도
-95°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to warm to -10° C.
  2. 2
    기타The cold bath was removed
  3. 3
    workup.ADDITION2N HCl was added
  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, 99:1)

실험 절차

3-Iodo-4-methylpyridine (330 mg, 3.10 mmol) was dissolved in Et2O and cooled to -95° C. A solution of t-BuLi (1.7M in pentane, 4.0 ml, 6.80 mmol) in pentane was added dropwise. 1,2,3,5,6,7-hexahydropyrrolizinium perchlorate (960 mg, 4.60 mmol) was added, and the reaction mixture was allowed to warm to -10° C. with stirring for 2 hours. The cold bath was removed, 2N HCl was added, and the phases were separated. The aqueous phase was basified with 15% NaOH and extracted with CH2Cl2 (2×). The CH2Cl2 fractions were combined, dried (MgSO4) and concentrated, and the residue was chromatographed (silica gel; CHCl3 /MeOH, 99:1) to afford the title compound as an oil (41 mg, 6%): 1H NMR (CDCl3, 300 MHz) δ1.54-1.69 (m, 2H), 1.77-1.89 (m, 2H), 1.93-2.11 (m, 4H), 2.41 (s, 3H), 2.69-2.77 (m, 2H), 3.08-3.15 (m, 2H), 7.02 (d, J=4.8 Hz, 1H), 8.32 (d, J=4.8 Hz, 1H), 9.06 (s, 1H); MS (CI/NH3) m/z: 203 (M+H)+.

출처

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