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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364925Generated: November 1, 2026

1,1',1''-(Chlorosilylidyne)tris(benzene) → HCID 59469955, compound

https://huagongshe.com/reaction/2364925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
ReactantChlorotriethylsilaneHCID 13819—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3,6-DibromocarbazoleHCID 274874—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59469955HCID 5946995566%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3,6-dibromocarbazole (9.1 g, 1 eq) in dry THF (400 ml) at 0° C. under argon is admixed slowly with NaH (60% in mineral oil, 1.3 g, 1.2 eq) and stirred at 0° C. for 2 h. After adding a solution of chlorotriethylsilane (5.1 g, 1.2 eq) in dry THF (80 ml), the solution is stirred at RT (room temperature) for 1 h. The solution is cooled to −78° C. and admixed with n-butyllithium (1.6 M in hexane, 43.8 ml, 2.5 eq) and stirred at −78° C. for 1 h. After adding a solution of chlorotriphenylsilane (29.8 g, 3.5 eq) in dry THF (100 ml) at −78° C., the mixture is warmed to room temperature overnight with stirring. Excess butyllithium is hydrolyzed with saturated ammonium chloride solution. The precipitated product is filtered off and washed thoroughly with methylene chloride. The combined methylene chloride filtrates are extracted by shaking with water and dried over sodium sulfate. The organic phase is admixed with tetra-n-butylammonium fluoride (TBAF, 1 M in THF, 2 ml) and stirred at RT for 4 h. The mixture is concentrated down to 100 ml. The resulting precipitate is filtered and washed with n-hexane. Yield 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697255B2
Source datasetuspto-grants-2014_04
ORD IDord-f71db7a5f70c4737b0674cdd3991713f
Source noteuspto-grants-2014_04