Реакция #1435686

Уравнение реакции

magnesium

TEOS

1,4-dibromobenzene

iodine

→

1,4-bis(triethoxysilyl)benzene

Выход 43.0%

Растворители

THF

THF

THF

Условия реакции

Обработка

1. 1
   Другоеwere placed under nitrogen in a 1 L three-neck round bottom flask
2. 2
   Другоеequipped with magnetic stir bar, condenser, and addition funnel
3. 3
   Температураto reflux
4. 4
   workup.ADDITIONthe addition
5. 5
   Температураat reflux for 1 h
6. 6
   Другоеwas removed in vacuo
7. 7
   workup.ADDITIONHexane (200 mL) was added
8. 8
   Другоеto precipitate any remaining magnesium salts in solution
9. 9
   Фильтрацияthe mixture was quickly filtered under nitrogen
10. 10
    Другоеto produce a clear, light brown solution
11. 11
    ДругоеHexane was removed in vacuo
12. 12
    workup.DISTILLATIONThe product was purified by fractional distillation
13. 13
    ДругоеThe product was recovered as a clear liquid at 130–5° C. (0.2 mmHg) in 43–47% yield

Методика

A mixture of magnesium turnings (15 g) and TEOS (450 mL, 2 mol) in THF (300 mL) were placed under nitrogen in a 1 L three-neck round bottom flask equipped with magnetic stir bar, condenser, and addition funnel. A small crystal of iodine was added and the mixture was brought to reflux. A solution of 1,4-dibromobenzene (48 g, 204 mmol) in THF (100 mL) was added dropwise over 2 h. Within 30 min of initiating the addition, the reaction became mildly exothermic. The reaction mixture was kept at reflux for 1 h after the completion of the addition of dibromide. The gray-green mixture was allowed to cool to room temperature before the THF was removed in vacuo. Hexane (200 mL) was added to precipitate any remaining magnesium salts in solution and the mixture was quickly filtered under nitrogen to produce a clear, light brown solution. Hexane was removed in vacuo. The product was purified by fractional distillation. The product was recovered as a clear liquid at 130–5° C. (0.2 mmHg) in 43–47% yield. 1H NMR (500 MHz, CDCl3) δ 7.67 (s, 4H, ArH), 3.86 (q, J=7.00 Hz, 12H, OCH2CH3), 1.23 (t, J=7.00 Hz, 18H, ArH); 13C NMR (125 MHz, CDCl3) δ 133.25,57.98, 17.43; 29Si NMR (99 MHz, CDCl3) δ−58.25; MS m/e calc'd for CI (M) C18H34Si2O6: 402.1894, found 402.1886.

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