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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197901Generated: October 30, 2026

Chlorotrimethylsilane → N-(4-Ethenylphenyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine

https://huagongshe.com/reaction/1197901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantN-(4-Ethenylphenyl)-1,1,1-trimethylsilanamineHCID 19365477—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-Ethenylphenyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamineHCID 2129271555%

Reaction Steps

To a solution of ethylmagnesium bromide in THF (0.6M, 150 mL) was added dropwise 4-[N-(trimethylsilyl)amino]styrene (8.4 g, 44 mmole) with stirring. The mixture was stirred at 40° C. for 16 hours. To the resulting solution was added trimethylsilylchloride (13 g, 120 mmole)and the mixture stirred at room temperature for 6 hours. By fractional distillation, a product was isolated at 45°-48° C./0.32 mm in 55% yield. The product was confirmed by spectral analysis to be the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278244
Source datasetuspto-grants-1994_01
ORD IDord-df77590464f54e25aecb66a4ca71d461
Source noteuspto-grants-1994_01