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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270735생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/270735

반응식

참여 물질

역할이름HCID투입량
반응물1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
반응물9,10-DibromoanthraceneHCID 68226—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물9-Bromo-l0-triphenysilyl anthraceneHCID 59833959—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449593B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-fecb7ac6bffa4b2094f2007780da8def
출처 메모uspto-grants-2008_11