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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1',1''-(Chlorosilylidyne)tris(benzene) | HCID 6458 | — |
| Reactant | 9,10-Dibromoanthracene | HCID 68226 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-Bromo-l0-triphenysilyl anthracene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07449593B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-fecb7ac6bffa4b2094f2007780da8def |
|---|
| Source note | uspto-grants-2008_11 |
|---|