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HRID 1672439作成日:2026年10月24日

Acetonitrile → 1-Trimethylsilanyloxy-4,5-dimethoxyindane-1-carbonitrile

https://huagongshe.com/ja/reaction/1672439

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Trimethylsilyl cyanideHCID 82115—
反応物4,5-Dimethoxy-1-indanoneHCID 240446—
触媒zinc(II)iodideHCID 9883512—
溶媒TolueneHCID 1140—
溶媒Sodium BicarbonateHCID 516892—
生成物1-Trimethylsilanyloxy-4,5-dimethoxyindane-1-carbonitrileHCID 6672466273%

反応条件

温度50 °C

反応手順

Under nitrogen, zinc iodide (1.5 g, 4.68 mmol), trimethylsilyl cyanide (27.1 mL, 203.0 mmol) were added sequentially to the solution of 4,5-dimethoxy-1-indanone (30.0 g, 156.1 mmol) in toluene (100 mL) and acetonitrile (24 mL). The reaction mixture was heated to 50° C. for 16 h. The reaction mixture was cooled to room temperature and diluted with 100 mL of toluene and 60 mL of a saturated aqueous sodium bicarbonate solution. After the mixture was stirred for 1 h, the layers were separated. The organic layer was washed by brine (60 mL) and dried (Na2SO4). The organic layer was concentrated in vacuo and the residue was purified by chromatography (EtOAc/Hexanes: 5/95) to afford 1-trimethylsilanyloxy-4,5-dimethoxyindane-1-carbonitrile (33.1 g, 73%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07998978B2
出典データセットuspto-grants-2011_08
ORD IDord-581e6cc5b894409ba8eb0381f926ec24
出典メモuspto-grants-2011_08