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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275083Generated: October 25, 2026

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

https://huagongshe.com/reaction/275083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDichlorodimethylsilaneHCID 6398—
ReactantIndeneHCID 7219—
ReactantTetrahydrofuranHCID 8028—
SolventWaterHCID 962—
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 butylithium 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 numberUS05391790
Source datasetuspto-grants-1995_02
ORD IDord-f5c7c27cf2944810b530ef5b80a59d79
Source noteuspto-grants-1995_02