HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768560Generated: November 1, 2026
Chlorotrimethylsilane → (4-Ethylphenyl)trimethylsilane
https://huagongshe.com/reaction/1768560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1-Bromo-4-ethylbenzene | HCID 15313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Ethylphenyl)trimethylsilane | HCID 280168 | 93.5% |
Reaction Steps
Magnesium(9.5 g, 0.39 mole) was suspended in THF (60 mL) at room temperature. A solution of 4-bromo-1-ethylbenzene (49 mL, 0.36 mole) in 300 mL of THF was added dropwise at such a rate as to maintain the temperature between 30° and 60° C. When the addition was complete the reaction mixture was stirred for an additional hour and then cooled to 30° C. Trimethylsilyl chloride (49 mL, 0.39 mole) was added dropwise at such a rate as to maintain the temperature between 30° and 40° C. The thin suspension was stirred overnight at room temperature. Saturated aqueous NH4Cl was added and the reaction mixture partitioned. The aqueous phase was extracted three times with ether, and the combined organic phases were dried (MgSO4) and concentrated. The resultant oil (60 g, 93% yield) was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05378708 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-9aeb1ca2cefd4046b7d283a5ce4798e1 |
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| Source note | uspto-grants-1995_01 |
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