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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270735Generated: October 25, 2026

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

https://huagongshe.com/reaction/270735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
Reactant9,10-DibromoanthraceneHCID 68226—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product9-Bromo-l0-triphenysilyl anthraceneHCID 59833959—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449593B2
Source datasetuspto-grants-2008_11
ORD IDord-fecb7ac6bffa4b2094f2007780da8def
Source noteuspto-grants-2008_11