Water → Disiloxane, 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyl-

HRID 1248743

Reaktionsgleichung

Reaktionsgleichung von HRID 1248743
[Cl:1][CH2:2][CH2:3][CH2:4][Si:5](Cl)([CH3:7])[CH3:6].C(=O)([O-])[O-].[Na+].[Na+].[OH2:15]>>[Cl:1][CH2:2][CH2:3][CH2:4][Si:5]([CH3:7])([CH3:6])[O:15][Si:5]([CH2:4][CH2:3][CH2:2][Cl:1])([CH3:7])[CH3:6]

Komponenten

4

Versuchsvorschrift

To a triangular flask of 2 l containing 1200 ml of water was added dropwise 342 g of 3-chloropropylchlorodimethylsilane (hereinafter referred to as "CPCDMSi") in an hour while stirring with a magnetic stirrer at a room temperature. After completion of the addition, the reaction mixture was neutralized with sodium carbonate and then extracted three times with each 500 ml of n-hexane. After drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane was removed under reduced pressure. The obtained residue was distilled under reduced pressure, and then the distillate obtained at 103° C./1.5 mmHg was collected to give 255 g (Yield 89%) of 1,3-bis(3-chloropropyl)-1,1,3,3-tetramethyldisiloxane (hereinafter referred to as "BCPSi").

Aufarbeitung

  1. customin an hour
  2. additionAfter completion of the addition
  3. extractionextracted three times with each 500 ml of n-hexane
  4. dry with materialAfter drying the n-hexane layer with anhydrous magnesium sulfate, n-hexane
  5. customwas removed under reduced pressure
  6. distillationThe obtained residue was distilled under reduced pressure
  7. customthe distillate obtained at 103° C./1.5 mmHg
  8. customwas collected

Quellen und Nachweise

ORD-Eintrag
ord-183c214edbe94ae8a1b2f00cd9c726de
Quelldatensatz
uspto-grants-1985_06
Patentnummer
US04525563

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