Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1',1''-(Chlorosilylidyne)tris(benzene)HCID 6458—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 66661151HCID 66661151—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59720465HCID 5972046574%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08373159B2
Source datasetuspto-grants-2013_02
ORD IDord-e8169a3374a24c7486609b90530d0561
Source noteuspto-grants-2013_02