تفاعل #517917

ord-82500da7314442d68968a70b0519e0e6

معادلة التفاعل

c1scc2c1OCCO2
EDOT
[Li][CH2]CCC
nBuLi
CCC[CH2][Sn]([Cl])([CH2]CCC)[CH2]CCC
Bu3SnCl
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
2-Tributylstannyl-3,4-ethylenedioxythiophene

المتفاعلات

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06323309B1uspto-grants-2001_11