Reaktion #324032

ord-88e552d6ce6545089f524dc47090fe0f

Reaktionsgleichung

Cl[Si](Cl)(c1ccccc1)c1ccccc1
diphenyldichlorosilane
Cl[SiH](Cl)Cl
trichlorosilane
C[CH2][Al+][CH2]C.[Cl-]
diethylaluminum chloride
Cl
hydrogen chloride
C[Si](C)(C)Cl
trimethylchlorosilane
C[Si](C)(Cl)c1ccccc1
phenyldimethylchlorosilane
Cl[SiH2]C(c1ccccc1)c1ccccc1
diphenylmethylchlorosilane
Cl[Si](c1ccccc1)(c1ccccc1)c1ccccc1
triphenylchlorosilane

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeInto a 3-necked flask equipped with a stirrer
  2. 2
    Temperaturreflux condenser
  3. 3
    workup.ADDITIONa gas conduit, is introduced over a period of 5 minutes with constant agitation and at room temperature
  4. 4
    Sonstigemeasured at 20° C.
  5. 5
    Temperaturis heated
  6. 6
    Temperaturunder reflux
  7. 7
    workup.DISTILLATIONFractional distillation

Vorschrift

Into a 3-necked flask equipped with a stirrer, reflux condenser and a gas conduit, is introduced over a period of 5 minutes with constant agitation and at room temperature, 2-liters [measured at 20° C. and 720 mm Hg (abs.) and thus 0.94 percent based on the total weight of the silanes used], of gaseous hydrogen chloride, into a mixture consisting of 253 grams (1 mol) of diphenyldichlorosilane, 88 grams (1 mol) of tetramethylsilane, 3 grams of trichlorosilane and 3 grams diethylaluminum chloride. Stirring is continued for an additional 4 hours while the mixture is heated under reflux. Fractional distillation yields 30 grams of trimethylchlorosilane, 35 grams of phenyldimethylchlorosilane, 80 grams of diphenylmethylchlorosilane and 74 grams of triphenylchlorosilane.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04158010uspto-grants-1979_06