Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Allylchlorodimethylsilane | HCID 77646 | — |
| Reactant | 2-(2-Bromoethyl)-1,3-dioxolane | HCID 87776 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57659389 | HCID 57659389 | — |
Reaction Steps
To a slurry of magnesium (2.43 g) in dry tetrahydrofuran (50 mL), few drops of dibromoethane (˜50 μL) was added under argon and stirred at room temperature for 10 min. The reaction mixture was cooled to 10° C. and 2-(2-bromoethyl)-1,3-dioxolane (10.9 g) was introduced dropwise during 10 min and allowed to stir at room temperature for 2 hours. The resulting reaction mixture was cooled to −10° C. and allyldimethylchlorosilane (6.73 g) was added dropwise during 10 min. and stirred over night at room temperature. Finally, the reaction content was quenched with aqueous NaHCO3 (15 mL) and extracted with ether (3×50 mL). The combined organic layer was dried and concentrated under mild vacuum to obtain the crude product, which was advanced to the next step without further purification (yield 9.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07687496B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-7394fa015b1347c9a15e28d54897c96a |
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| Source note | uspto-grants-2010_03 |
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