반응 #3428
ord-5b22770333014a4da72ab520662759f7
반응 방정식
반응 조건
온도
-30°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.STIRRINGto stir for 30 minutes at -30° C.
- 2온도to warm to room temperature
- 3workup.STIRRINGstir for 1 hour
- 4기타the phases were separated
- 5추출extracted with CH2Cl2 (2×)
- 6건조dried (MgSO4)
- 7농축concentrated
- 8기타the 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).