HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493461Generated: October 26, 2026
Silane, trimethyl((1-methylethenyl)oxy)- → (4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane
https://huagongshe.com/reaction/493461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Silane, trimethyl((1-methylethenyl)oxy)- | HCID 74599 | — |
| Reactant | HCID 57681726 | HCID 57681726 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | (4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane | HCID 57681748 | 43.2% |
Reaction Steps
To a cooled (0° C.) solution of MeLi (13.0 mL; 21 mmol; 1.6 M in Et2O) was added 2-(trimethylsilyloxy)propene (2.8 g; 21 mmol). The solution was stirred 30 minutes at 0° C., and then warmed to room temperature and was stirred for 1 hour. The mixture was recooled to 0° C., and (4R,5R)-2-allyl-2-chloro-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolane (6.6 g; 21 mmol) was added. The mixture 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 3.0 g (43%) of (4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[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-395477f10ae54dd890ad556b2871b438 |
|---|
| Source note | uspto-grants-2009_05 |
|---|