HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl Acetate → Tetraethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl Acetate | HCID 7904 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Ethenyltriethylsilane | HCID 559195 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tetraethylsilane | HCID 12426 | — |
| Product | Triethylsilanol | HCID 69005 | — |
Reaction Steps
In a reactor were placed di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [IrCl(cod)]2 (0.05 mmol), vinyl acetate (20 mmol), and toluene (3 ml). The mixture was raised in temperature to 40° C. in a nitrogen atmosphere, triethylsilane (Et3SiH) (5 mmol) was added thereto over one hour, and a reaction was carried out at 40° C. for one hour. After the reaction, the reaction mixture was analyzed by gas chromatography to find that vinyltriethylsilane was produced in a yield of 36% and tetraethylsilane and acetic ester of triethylsilanol were by-produced in yields of 7% and 12%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745654B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-c37ee7496bef4a1ba95597d93832f390 |
| Source note | uspto-grants-2010_06 |