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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840694Generated: October 30, 2026

Trimethylsilylacetylene → Tris(4-((trimethylsilyl)ethynyl)phenyl)amine

https://huagongshe.com/reaction/1840694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantTris(4-bromophenyl)amineHCID 258027—
CatalystCopper iodideHCID 83717—
SolventDiisopropylamineHCID 7912—
ProductTris(4-((trimethylsilyl)ethynyl)phenyl)amineHCID 2344370781%

Reaction Steps

Thereafter, to 200 ml of diisopropylamine were added 15.54 g (0.032 mol of tri(4-bromophenyl)amine, 1.35 g (1.92 mmol) of bis[triphenylphosphin]palladium dichloride and 9.43 g (0.96 mmol) of copper iodide. After the reaction mixture was stirred for 2 h at room temperature, 9.43 g, (96 mmol) of trimethylsilyl acetylene was slowly added to the reaction mixture. The reaction mixture was refluxed for 8 h and cooled. Solvent was removed under the reduced pressure. The residue was extracted with benzene and the benzene layer was washed with distilled water. The washed benzene layer was concentrated to give 13.84 g (81%) of tri(4-trimethylsilylethynylphenyl)amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06682782B2
Source datasetuspto-grants-2004_01
ORD IDord-c28251a72e284fd682b010ce47b24c90
Source noteuspto-grants-2004_01