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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375928Generated: October 26, 2026

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

https://huagongshe.com/reaction/1375928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDichlorodimethylsilaneHCID 6398—
Reactant1H-Indene, 2-methyl-HCID 16587—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl-bis(2-methyl-1H-inden-1-yl)silaneHCID 4050248—

Reaction Conditions

Temperature80 °C

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169864B2
Source datasetuspto-grants-2007_01
ORD IDord-d3b03266a7394bfaa66e3536a76eb3fd
Source noteuspto-grants-2007_01