HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → N-(4-Ethenylphenyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | N-(4-Ethenylphenyl)-1,1,1-trimethylsilanamine | HCID 19365477 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Ethenylphenyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine | HCID 21292715 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278244 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-df77590464f54e25aecb66a4ca71d461 |
| Source note | uspto-grants-1994_01 |