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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364926Generated: November 2, 2026

1,1',1''-(Chlorosilylidyne)tris(benzene) → HCID 58131163, compound

https://huagongshe.com/reaction/2364926

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3,6-DibromocarbazoleHCID 274874—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58131163HCID 58131163—

Reaction Steps

NaH (60% dispersion in oil, 1.5 g, 37 mmol) is added slowly to a cold solution (0° C.) of 3,6-dibromocarbazole (10.4 g, 31 mmol) in dry THF (1000 ml). After stirring for two hours, a solution of ClSiPh3 (18.7 g, 62 mmol) in dry THF (200 ml) is added at 0° C. 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. Filtration through SiO2 gives the desired product (quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697255B2
Source datasetuspto-grants-2014_04
ORD IDord-1e065c14a75a420eac7d72849ee23323
Source noteuspto-grants-2014_04