반응 #517917

ord-82500da7314442d68968a70b0519e0e6

시약

없음

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was removed under vacuum
  2. 2
    여과The slurry was filtered through Celite
  3. 3
    기타the amber filtrate was removed under vacuum
  4. 4
    기타to yield a yellow-orange oil which
  5. 5
    workup.DISTILLATIONwas purified by distillation (b.p. 120° C./30 mTorr)
  6. 6
    기타to yield 79.6 g (185, mmol 98%) of pale yellow oil

실험 절차

A structure of the product is depicted schematically in FIG. 13. To a cold (−15° C.) solution of 3,4-ethylenedioythiophene (EDOT) (20 ml, 188 mmol) in 350 mL of THF were slowly added 138 mL (207 mmol, 1.1 equiv) of nBuLi. The white slurry was allowed to stir at −15° C. for 3 h before the addition of 61.6 mL (227 mmol, 1.2 equiv) of Bu3SnCl. The beige slurry was allowed to stir while warming to room temperature for 18 h. The solvent was removed under vacuum and then stiffed in hexane for 30 min. The slurry was filtered through Celite and the amber filtrate was removed under vacuum to yield a yellow-orange oil which was purified by distillation (b.p. 120° C./30 mTorr) to yield 79.6 g (185, mmol 98%) of pale yellow oil. 1H NMR (CDCl3) δ6.57 (s, 1H), 4.20-4.10 (m, 4H), 1.62-1.50 (m, 6H), 1.40-1.25 (m, 6H), 1.12-1.06 (m, 6H), 0.89 (t, 3H). MS m/z 433 (M+H+); HRMS (FAB) m/z 433.1225 (M+H+); calcd for C18H32O2SSn m/z 433.1223 (M+H+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06323309B1uspto-grants-2001_11