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Chlorotrimethylsilane → Silane, (4-bromophenyl)trimethyl-

HRID 64621
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 64621
[Br:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[CH:4][CH:3]=1.C([Li])CCC.[CH3:14][Si:15]([CH3:18])([CH3:17])Cl>CCOCC.CCCCCC>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Si:15]([CH3:18])([CH3:17])[CH3:14])=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 6397ChlorotrimethylsilaneHCID 78041,4-DibromobenzeneHCID 178418339Butyllithium

Produkt 1

HCID 138897Silane, (4-bromophenyl)trimethyl-

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittel2×HCID 8058Hexane
Lösungsmittel

Versuchsvorschrift

Under argon, 94.4 g of p-dibromobenzene is cooled to -20° C. in 400 ml of absolute ether. To the solution is added dropwise 255 ml of 15% butyllithium in hexane so that the temperature does not rise above -10° C. Then the mixture is agitated for one hour at room temperature. After a negative Gilman test (H. Gilman, J. Swiss, J. Amer. Chem. Soc. 62: 1847 [1940]), the mixture is again cooled to -20° C. and 46 ml of trimethylchlorosilane in 200 ml of absolute ether is added dropwise thereto so that the temperature does not exceed -10° C. After the addition step is finished, the mixture is stirred for 16 hours at room temperature and another hour under reflux. The thus-formed precipitate is suctioned off and thoroughly washed with ether. The resultant filtrate is concentrated and then distilled with a water-jet aspirator, thus producing 65.52 g of p-bromotrimethylsilylbenzene, bp (16 torr) 103°-110° C.

Aufarbeitung

  1. customdoes not rise above -10° C
  2. temperatureAfter a negative Gilman test (H. Gilman, J. Swiss, J. Amer. Chem. Soc. 62: 1847 [1940]), the mixture is again cooled to -20° C.
  3. customdoes not exceed -10° C
  4. additionAfter the addition step
  5. stirringthe mixture is stirred for 16 hours at room temperature and another hour
  6. temperatureunder reflux
  7. washthoroughly washed with ether
  8. concentrationThe resultant filtrate is concentrated
  9. distillationdistilled with a water-jet aspirator

Quellen und Nachweise

ORD-Eintrag
ord-380ef2b45f9e43889dd62b604dbfb785
Quelldatensatz
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04609651

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