HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 19601754, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | HCID 102356231 | HCID 102356231 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19601754 | HCID 19601754 | 43.9% |
Reaction Steps
Hydrosilation of phenylacetylene with bis(dichlorosilyl)trichlorosilylmethane in the presence of Pt(C2H4)(PPh3)2. Into the same apparatus as described in Example 1 were add 0.99 g of bis(dichlorosilyl)trichlorosilylmethane, 0.101 g of Pt(C2H4)(PPh3)2, and 25 ml of dried benzene forming a mixture. To this mixture at reflux was added 0.32 ml of phenylacetylene over a 10 minute period. The resulting mixture was stirred for an additional 15 hours at reflux temperature and then the solvent removed. The residue was vacuum distilled at 67 Pa to give a mixture comprising 0.58 g of 1,1,3,3-tetrachloro-2-trichlorosilyl-4-phenyl-1,3-disilacyclopent-4-ene (TCD-GC area 43.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998649 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-cafd29a8814d41ccafb3a668a2cc600e |
| Source note | uspto-grants-1999_12 |