HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl triflate → (3-Ethoxy-1-methylene-allyloxy)-trimethyl-silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | 4-Ethoxy-but-3-en-2-one | HCID 15871655 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Ethoxy-1-methylene-allyloxy)-trimethyl-silane | HCID 85441339 | 77.5% |
Reaction Steps
In a 250 mL three-necked flask under N2 atomosphere, to a solution of 7.2 g of 4-ethoxy-but-3-en-2-one (63 mmol, 1 eq) and 12.7 g of TEA (126 mmol, 2 eq) in THF at −78° C., was added 21 g of TMSOTf (95 mmol, 1.5 eq) dropwise in 40 mins. Stirring was continued for 60 mins at 0˜−30° C. After the conversion was complete (check by NMR), the reaction was quenched with 5% NaHCO3, extract with Hexane and dried over Na2SO4. After remove the solvent the crude product was purified with redistillation (oil pump, <<1 mmbar: Bp, 40° C., Toluene; Bp, 115° C., product) to give 9.1 g pure product. Yield: 72.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553833B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-482f8fbfd6d340628d79f328486af323 |
| Source note | uspto-grants-2009_06 |