HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387611Generated: October 30, 2026
1,1',1''-(Chlorosilylidyne)tris(benzene) → HCID 59720465, compound
https://huagongshe.com/reaction/387611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1',1''-(Chlorosilylidyne)tris(benzene) | HCID 6458 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 66661151 | HCID 66661151 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59720465 | HCID 59720465 | 74% |
Reaction Steps
A solution of 9-(3-methoxyphenyl)-3,6-dibromo-9H-carbazole (26 g, 1 eq) in dry THF (700 ml) is admixed slowly at −78° C. under argon with n-butyllithium (1.6 M in hexane, 41 ml, 1 eq) and stirred at −78° C. for 2 h. After a solution of chlorotriphenylsilane (30 g, 1.5 eq) in dry THF (150 ml) had been added at −78° C., the mixture was warmed to room temperature overnight with stirring. Excess butyllithium is hydrolyzed with saturated ammonium chloride solution. The precipitated reaction product is filtered off and washed thoroughly with methylene chloride. The combined methylene chloride filtrates are extracted with water and concentrated to dryness. The residue is stirred with acetone and filtered off. Yield 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08373159B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-e8169a3374a24c7486609b90530d0561 |
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| Source note | uspto-grants-2013_02 |
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