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HRID 270735作成日:2026年10月26日

1,1',1''-(Chlorosilylidyne)tris(benzene) → 9-Bromo-l0-triphenysilyl anthracene

https://huagongshe.com/reaction/270735

反応式

関与物質

役割名称HCID仕込み量
反応物1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
反応物9,10-DibromoanthraceneHCID 68226—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物9-Bromo-l0-triphenysilyl anthraceneHCID 59833959—

反応手順

In a nitrogen atmosphere, 12 g (35.7 mmol) of 9,10-dibromoanthracene, and 300 ml of tetrahydrofuran (THF) were added to a round-bottom flask. Next, 14.4 ml (35.7 mmol, 2.5M) of n-butyl lithium was added dropwise slowly into the round-bottom flask at −78° C. After mixing and reacting for 30 min, 12 g (40.7 mmol) triphenylsilyl chloride with 50 ml THF were added dropwise slowly into the round-bottom flask at −78° C. After reacting at room temperature for 24 hours, the resulting mixture was subjected to extraction with a mixed solvent (ethyl acetate:H2O), dried over anhydrous MgSO4, filtered, and condensed, then the crude product was purified by column chromatography (n-hexane/acetyl acetate=15/1), A 9.0 g of pure 9-bromo-10-triphenysilyl anthracene was collected.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449593B2
出典データセットuspto-grants-2008_11
ORD IDord-fecb7ac6bffa4b2094f2007780da8def
出典メモuspto-grants-2008_11