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HRID 493461Erstellt: 26. Oktober 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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSilane, trimethyl((1-methylethenyl)oxy)-HCID 74599—
EduktHCID 57681726HCID 57681726—
EduktHCID 178418348HCID 178418348—
LösungsmittelPentaneHCID 8003—
Produkt(4R,5R)-2-allyl-2-isopropenyloxy-4,5-bis-(1-methoxy-1-methyl-ethyl)-[1,3,2]dioxasilolaneHCID 5768174843,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534905B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-395477f10ae54dd890ad556b2871b438
Quellennotizuspto-grants-2009_05