تفاعل #517916

ord-0e43f0457aba4390adf4b0bd2b7ece16

معادلة التفاعل

CCC[CH2][Sn]([Cl])([CH2]CCC)[CH2]CCC
tributylstannyl chloride
c1scc2c1OCCO2
3,4-ethylenedioxythiophene
[Li][CH2]CCC
n-butyl lithium
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1scc2c1OCCO2
2-(tributylstannyl)-3,4-ethylenedioxythiophene
المردود 99.4%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas warmed to room temperature
  2. 2
    أخرىThe solvent was removed by rotary evaporation
  3. 3
    workup.STIRRINGafter stirring for 8 h
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in hexanes
  5. 5
    ترشيحfiltered
  6. 6
    أخرىThe filtrate was dried in vacuum

الإجراء التجريبي

The synthesis described herein is depicted schematically in FIG. 4. 2.0 g (14 mmol) of 3,4-ethylenedioxythiophene in 150 ml dry THF was treated dropwise with 10 ml (16.2 mmol) of 1.6 M n-butyl lithium at −78° C. under argon. After stirring for 0.5 h and warming to −40° C., 5.95 g (18.8 mmol) tributylstannyl chloride was added to the solution and it was warmed to room temperature. The solvent was removed by rotary evaporation after stirring for 8 h. The residue was dissolved in hexanes and filtered. The filtrate was dried in vacuum to afford 6.0 g 2-(tributylstannyl)-3,4-ethylenedioxythiophene as a yellow liquid. The compound was used for next step reaction as obtained, no further purifications. 1H NMR (250 MHZ, CDCl3): d (ppm) 6.56 (s, 1H); 4.16 (s, 4H); 1.61-1.49 (m, 6H); 1.39-1.22 (m, 6H); 1.09 (t, 9H); 0.90 (q, 6H). 13C NMR (125 MHZ, CDCl3): d (ppm) 147.88, 142.65, 109.08, 105.99, 64.86, 64.80, 29.08, 27.40, 13.79, 10.71. (M+H)+ found: 431, caled for C18H32O2SSn: 430.11

المصدر

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