HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl acetate → Tetraethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl acetate | HCID 11584 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Tetrafluoroborate | HCID 26255 | — |
| Reactant | Allyltriethylsilane | HCID 11194462 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tetraethylsilane | HCID 12426 | 5% |
Reaction Steps
In a reactor were placed bis(1,5-cyclooctadiene)iridium tetrafluoroborate [Ir(cod)2]+BF4− (0.05 mmol), allyl acetate (20 mmol), and toluene (3 ml). The mixture was raised in temperature to 80° C. in a nitrogen atmosphere, triethylsilane (Et3SiH)(5 mmol) was added thereto over one hour, and a reaction was conducted at 80° C. for one hour. After the reaction, the reaction mixture was analyzed by gas chromatography to find that allyltriethylsilane was produced in a yield of 54% and tetraethylsilane was by-produced in a yield of 5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745654B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-49ca4e2f681548ffad2587d89196df70 |
| Source note | uspto-grants-2010_06 |