Reaktion #628147

Reaktionsgleichung

trimethyltin chloride

thieno[3,2-b]thiophene

n-BuLi

hexane

→

crystals

Ausbeute 82.0%

2,5-bis(trimethylstannyl)thieno[3,2-b]thiophene

Ausbeute 82.0%

Lösungsmittel

CHCl3

water

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGAfter stirring at −50° C. for 2 h
2. 2
   Temperaturthe solution was warmed to room temperature
3. 3
   workup.STIRRINGstirred for 24 h
4. 4
   WaschenThe organic layer was washed twice with 50 mL of water
5. 5
   Trocknendried over anhydrous Na2SO4
6. 6
   SonstigeThe organic layer was evaporated
7. 7
   Sonstigedried over vacuum
8. 8
   Sonstigeto afford brown solid
9. 9
   SonstigeThe solid was then purified by recrystallization from Et2O

Vorschrift

To a solution of thieno[3,2-b]thiophene (1.2 g, 8.56 mmol) in 60 mL THF, 2.5 M solution of n-BuLi in hexane (7.25 mL, 18.0 mmol) was added dropwise at −50° C. under N2. The solution was stirred at −50° C. for 2 h and 1.0 M solution of trimethyltin chloride (18.9 mL, 18.8 mmol) in THF was added in one portion. After stirring at −50° C. for 2 h, the solution was warmed to room temperature and stirred for 24 h. The resulting mixture was poured into deionized water and 100 mL of CHCl3. The organic layer was washed twice with 50 mL of water and dried over anhydrous Na2SO4. The organic layer was evaporated and dried over vacuum to afford brown solid. The solid was then purified by recrystallization from Et2O to give colourless crystals (0.6 g, 82% yield). 1H NMR (CDCl3, 300 MHz, ppm): δ 7.26 (s, 2H), 0.48 (s, 18H).

Quelle