HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → Dichloro[(dichlorosilyl)methyl](2-phenylethenyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Bisdichlorosilylmethane | HCID 57370748 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dichloro[(dichlorosilyl)methyl](2-phenylethenyl)silane | HCID 71376014 | 27.3% |
Reaction Steps
Hydrosilation of phenylacetylene with bis(dichlorosilyl)methane in the presence of H2PtCl6 /THF. Into the same apparatus as described in Example 1 were added 1 g of bis(dichlorosilyl)methane, 20 μl of 0.1 M H2PtCl6 in THF (tetrahydrofuran) solution, 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 8 hours and then the solvent removed at atmospheric pressure. The products were vacuum distilled at 67 Pa to give a mixture comprising 1.66 g of 3,3,5,5-tetrachloro-1-phenyl-3,5-disilapenta-1-ene (TCD-GC area 27.3%) and 3,3,5,5-tetrachloro-1,7-diphenyl-3,5-disilahepta-1,6-diene (TCD-GC area 26.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998649 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-4de2b1b3a328468aaa621dca56360a30 |
| Source note | uspto-grants-1999_12 |