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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376938Generated: October 31, 2026

Chlorotrimethylsilane → HCID 22918073, compound

https://huagongshe.com/reaction/1376938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium BicarbonateHCID 516892—
ReactantCyclotetrasilane, octaethyl-HCID 529608—
ReactantHCID 178506967HCID 178506967—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 22918073HCID 2291807347%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663271
Source datasetuspto-grants-1997_09
ORD IDord-d6899ed64e374826a17eebbc9c44a5f4
Source noteuspto-grants-1997_09