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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52676Generated: October 25, 2026

Toluene → di(1H-inden-1-yl)dimethylsilane

https://huagongshe.com/reaction/52676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDichlorodimethylsilaneHCID 6398—
ReactantIndeneHCID 7219—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productdi(1H-inden-1-yl)dimethylsilaneHCID 59942997%

Reaction Steps

Technical-grade indene (90%) was first filtered through aluminum oxide (superactive) for crude purification and drying. 160 ml (400 mmol) of a 2.5M butyllithium solution in hexane were added at room temperature to a solution of 57 ml (446 mmol) of the indene (91-92%) in a solvent mixture comprising 430 ml of toluene and 32 ml of THF, and the mixture was refluxed for 1 hour. The mixture was cooled to room temperature, and 24.2 ml (200 mmol) of dimethyldichlorosilane were added to the orange suspension. The mixture was refluxed for 5 hours and subsequently poured into water. The mixture was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate and freed from solvent under reduced pressure. The residue which remained was dried for several hours in an oil-pump vacuum at 50° C. 56 g (97%) of the ligand system 1 were obtained as a brownish oil (isomer mixture, 2 diastereomers, 1 double-bond isomer). The isomer mixture can be used directly for the preparation of the metallocene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616747
Source datasetuspto-grants-1997_04
ORD IDord-f8379401396b4cbe8443806467d665b2
Source noteuspto-grants-1997_04