Reaktion #697901

ord-6c47efcc63f2450cb363cc528d8e7fd3

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto form a mixture
  2. 2
    workup.ADDITIONwere added over a 30 minute period
  3. 3
    Temperaturat reflux temperature for an additional 18 hours
  4. 4
    Sonstigethe solvent removed at atmospheric pressure
  5. 5
    workup.DISTILLATIONdistilled

Vorschrift

Hydrosilation of diphenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pd(PPh3)4. Into the same apparatus as described in Example 1 were add 0.98 g of bis(dichlorosilyl)trichlorosilylmethane, 0.101 g of Pd(PPh3)4, and 25 ml of dried benzene to form a mixture. The mixture was brought to reflux temperature and 0.52 g of diphenylacetylene in 10 ml of benzene were added over a 30 minute period. The mixture was stirred at reflux temperature for an additional 18 hours and then the solvent removed at atmospheric pressure. The residue was vacuum distilled to yield a mixture comprising 0.417 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-4,5-diphenyl-1,3-disilacyclopentane (TCD-GC area 25%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05998649uspto-grants-1999_12