HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376938Generated: October 31, 2026
Chlorotrimethylsilane → HCID 22918073, compound
https://huagongshe.com/reaction/1376938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Cyclotetrasilane, octaethyl- | HCID 529608 | — |
| Reactant | HCID 178506967 | HCID 178506967 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 22918073 | HCID 22918073 | 47% |
Reaction Steps
In an argon atmosphere, to a tetrahydrofuran solution (1 ml) of 52 mg (0.15 mmol) of octaethylcyclotetrasilane was added 0.56 ml (0.15 mmol) of a tetrahydrofuran solution (0.27M) of phenyldimethylsilyllithium, and stirred at 0° C. for 15 minutes. Trimethylchlorosilane in an amount of 108 mg (1.0 mmol) was added, and reacted at room temperature for 3 hours. Hexane (2 ml) and saturated aqueous sodium bicarbonate solution (2 ml) were added, stirred, the hexane layer was separated, and dried with magnesium sulfate. The resulting crude product was purified by a silica gel column chromatography (hexane) to give 39 mg (47% yield) of 2,2,3,3,4,4,5,5-octaethyl-1,1,6,6,6-pentamethyl-1-phenylhexasilane (2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663271 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-d6899ed64e374826a17eebbc9c44a5f4 |
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| Source note | uspto-grants-1997_09 |
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