반응 #2784

ord-1d2b61ecfe914348bdf9551b97784846

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the solution was extracted with ether
  2. 2
    건조The ether phase was dried over MgSO4
  3. 3
    농축concentrated
  4. 4
    workup.WAITthe residue was left
  5. 5
    기타to crystallize at -35° C

실험 절차

12.3 cm3 (30.7 mmol) of a 2.5 molar hexane solution of n-butyllithium were slowly added to a solution of 5.10 g (30.7 mmol) of fluorene in 60 cm3 of tetrahydrofuran at room temperature. After 40 minutes, 7.07 g (30.7 mmol) of diphenylfulvene were added to the orange solution and the mixture was stirred overnight. 60 cm3 of water were added to the dark red solution, whereupon the solution became yellow in color, and the solution was extracted with ether. The ether phase was dried over MgSO4 and concentrated and the residue was left to crystallize at -35° C. 5.1 g (42%) of 1,1-cyclopentadienyl-(9-fluorenyl)diphenylmethane were obtained as a beige powder.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05731254uspto-grants-1998_03