HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → 1,3-Disilacyclopent-4-ene, 1,1,3,3-tetrachloro-4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Bisdichlorosilylmethane | HCID 57370748 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1,3-Disilacyclopent-4-ene, 1,1,3,3-tetrachloro-4-phenyl- | HCID 12121449 | 48.2% |
Reaction Steps
Hydrosilation of phenylacetylene with bis(dichlorosilyl)methane in the presence of Pd(PPh3)4. Into the same apparatus as described in Example 1 were added 1 g of bis(dichlorosilyl)methane, 0.101 g of Pd(PPh3)4, and 20 ml of dried benzene. The flask content was heated to reflux and 0.52 ml of phenylacetylene was added over a ten minute period. The flask content was refluxed, with stirring, for another hours and then the solvent removed at atmospheric pressure. The products were vacuum distilled at 67 Pa to give a mixture comprising 0.89 g of 1,1,3,3-tetrachloro-4-phenyl-1,3-disilacyclopent-4-ene (TCD-GC area 48.2%) and 3,3,5,5-tetrachloro-1,7-diphenyl-3,5-disilahepta-1,6-diene (TCD-GC area6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998649 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-6434ff18243b4d17b167d364b033792b |
| Source note | uspto-grants-1999_12 |