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HRID 52676作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/52676

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ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
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 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616747
出典データセットuspto-grants-1997_04
ORD IDord-f8379401396b4cbe8443806467d665b2
出典メモuspto-grants-1997_04