HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387614Generated: October 30, 2026
1,1',1''-(Chlorosilylidyne)tris(benzene) → HCID 58131120, compound
https://huagongshe.com/reaction/387614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1',1''-(Chlorosilylidyne)tris(benzene) | HCID 6458 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 58131163 | HCID 58131163 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58131120 | HCID 58131120 | — |
Reaction Steps
tert-BuLi (1.7 M in pentane, 58 ml, 99 mmol) is added slowly to a cold solution (−78° C.) of 3,6-dibromo-9-triphenylsilylcarbazole (90% purity, see i), 13 g, 22 mmol) in dry THF (1000 ml). After stirring at −78° C. for two hours, ClSiPh3 (34 g, 115 mmol) in dry THF is added. The mixture is stirred overnight, and saturated NH4Cl solution is added. The resulting salt is filtered off, and the organic phase is separated from the aqueous phase. The aqueous phase is extracted with CH2Cl2. The organic phase is washed twice with water. The combined organic phases are dried over Na2SO4. After column chromatography (SiO2; 5:1 cyclohexane:CH2Cl2), the pure product is obtained (Rf˜0.3, 11 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08373159B2 |
|---|
| Source dataset | uspto-grants-2013_02 |
|---|
| ORD ID | ord-b2e18cafc44449258b47267a1e40a487 |
|---|
| Source note | uspto-grants-2013_02 |
|---|