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HRID 275083作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/275083

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物DichlorodimethylsilaneHCID 6398—
反応物IndeneHCID 7219—
反応物TetrahydrofuranHCID 8028—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
生成物di(1H-inden-1-yl)dimethylsilaneHCID 59942997%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05391790
出典データセットuspto-grants-1995_02
ORD IDord-f5c7c27cf2944810b530ef5b80a59d79
出典メモuspto-grants-1995_02