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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 58131163HCID 58131163—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58131120HCID 58131120—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08373159B2
Source datasetuspto-grants-2013_02
ORD IDord-b2e18cafc44449258b47267a1e40a487
Source noteuspto-grants-2013_02