Reaktion #697901
ord-6c47efcc63f2450cb363cc528d8e7fd3
Reaktionsgleichung
Edukte
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeto form a mixture
- 2workup.ADDITIONwere added over a 30 minute period
- 3Temperaturat reflux temperature for an additional 18 hours
- 4Sonstigethe solvent removed at atmospheric pressure
- 5workup.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%).