HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylacetylene → HCID 19601750, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylacetylene | HCID 10390 | — |
| Reactant | HCID 102356231 | HCID 102356231 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19601750 | HCID 19601750 | 13.8% |
Reaction Steps
Hydrosilation of diphenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pt(C2H4)(PPh3)2. Into the same apparatus as described in Example 1 were added 0.99 g of bis(dichlorosilyl)trichlorosilylmethane, 0.102 g of Pt(C2H4)(PPh3)2, and 25 ml of dried benzene to form a mixture. To this mixture at reflux was added 0.52 g of diphenylacetylene in 10 ml of benzene over a 30 minute period. The resulting mixture was stirred for an additional 18 hours and then the solvent remove at atmospheric pressure. The residue was vacuum distilled at 67 Pa to yield a mixture comprising 0.61 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-4,5-diphenyl-1,3-disilacyclopentane (TCD-GC area 13.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998649 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-c212b91903904a459af565dce8159176 |
| Source note | uspto-grants-1999_12 |