Iodine → Diisopropyl(3-methoxypropyl)silane

HRID 1169568Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1169568
Br[CH2:2][CH2:3][CH2:4][O:5][CH3:6].[Mg].II.[CH:10]([SiH:13]([CH:15]([CH3:17])[CH3:16])Cl)([CH3:12])[CH3:11].[Cl-].[NH4+]>C1COCC1>[CH:10]([SiH:13]([CH:15]([CH3:17])[CH3:16])[CH2:2][CH2:3][CH2:4][O:5][CH3:6])([CH3:12])[CH3:11]

Komponenten

7

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

1-Bromo-3-methoxypropane (9.18 g, 60.0 mmol) was dissolved in THF (55 mL), and magnesium (1.53 g, 62.9 mmol) and iodine (catalytic amount) were added thereto, followed by stirring at room temperature for 20 minutes and at 55° C. for 5 minutes. The resultant mixture was added dropwise to diisopropylchlorosilane (8.88 mL, 52.0 mmol) in THF (65 mL) for 5 minutes, followed by stirring at room temperature for 1 hour. After termination of exothermic reaction, the resultant mixture was further stirred at 50° C. for 1.5 hours, and saturated aqueous ammonium chloride was added thereto. The resultant mixture was extracted with pentane, followed by washing with water six times and drying over sodium sulfate anhydrate. The solvent was removed under reduced pressure, whereby the Compound 60a was obtained as an yellow liquid (10.1 g, 89%).

Aufarbeitung

  1. stirringby stirring at room temperature for 1 hour
  2. customAfter termination of exothermic reaction
  3. extractionThe resultant mixture was extracted with pentane
  4. washby washing with water six times
  5. dry with materialdrying over sodium sulfate anhydrate
  6. customThe solvent was removed under reduced pressure, whereby the Compound 60a

Quellen und Nachweise

ORD-Eintrag
ord-5bd981af22ff45e48334337ac71934da
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07825103B2

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