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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1181616Erstellt: 27. Oktober 2026

Toluene → Dimethyl-bis(2-methyl-1H-inden-1-yl)silane

https://huagongshe.com/reaction/1181616

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktDichlorodimethylsilaneHCID 6398—
Edukt1H-Indene, 2-methyl-HCID 16587—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDimethyl-bis(2-methyl-1H-inden-1-yl)silaneHCID 4050248—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

8.0 g (61.4 mmoles) of 2-methylindene are introduced into 175 mL of toluene and 13 mL of THF, and 24.6 mL of n-butyllithium (2.5 M in toluene) are added without interruption at room temperature. After this addition is complete, the mixture is heated to 80° C. and stirred at this temperature for one hour. It is allowed to cool to 40° C., then 3.96 g (30.7 mmoles) of dimethyldichlorosilane are slowly added dropwise. After this addition, the reaction solution is stirred for three hours at 60° C. and then overnight at room temperature. 70 mL of water are added and the phases that form are separated. The organic phase is washed with 100 mL of water, and the aqueous phase is extracted three times with a total of 100 mL of toluene. The combined organic phases are dried over magnesium sulfate. After separation of the magnesium sulfate, the solvent is removed and the residue is purified by column chromatography. The desired product is isolated in a yield of 8.16 g (84%) (purity 99%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07285608B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-fac146bb6a2a488e83863c65a79b10f1
Quellennotizuspto-grants-2007_10