HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane → 2-Allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane | HCID 57681722 | — |
| Reactant | Trimethylvinyloxysilane | HCID 101265072 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 2-Allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane | HCID 11195542 | 72.3% |
Reaction Steps
To a cooled (0° C.) solution of MeLi (16.2 mL; 23 mmol; 1.4 M in Et20) was added trimethylvinyloxysilane (2.7 g; 23 mmol). The solution was warmed to room temperature and was stirred for 1 hour. The solution was cooled to −78° C., and 2-allyl-2-chloro-4,4,5,5-tetramethyl-[1,3,2]dioxasilolane (5.5 g; 25 mmol) was added. The solution was warmed to room temperature and stirred for 2 hours. The solution was diluted with pentane (20 mL), and the mixture was then filtered through a pad of celite. The filtrate was concentrated, and the residue was distilled under reduced pressure to give 3.8 g (70%) of 2-allyl-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane as a clear, colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534905B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-39a427f8a7a24e40bba5fb4f4b9d73fc |
| Source note | uspto-grants-2009_05 |