HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396108Generated: October 27, 2026
Chlorotrimethylsilane → 1,1-Bis(trimethylsilyl)ethanol
https://huagongshe.com/reaction/396108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Trimethylsilylacetate | HCID 22558220 | — |
| Product | 1,1-Bis(trimethylsilyl)ethanol | HCID 15351239 | 55% |
Reaction Steps
Trimethylchlorosilane (20.5 g, 190 mmol) is dissolved in 30 mL of tetrahydrofuran. The solution is suspended with sodium (6.50 g, 283 mmol) and then refluxed at 80° C. Under the argon atmosphere, trimethylsilylacetate (3.12 g, 23.6 mmol) in 20 mL of tetrahydrofuran is added via a syringe for an hour and then the solution is refluxed for another 30 minutes. Then, precipitated inorganic residue is filtered and solvent is removed under vacuum. Remained oil is separated by vacuum distillation to give 1,1-bis(trimethylsilyl)ethanol (yield: 55%). b.p. 110° C. (24 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06607867B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-f5616dcb27df401e81aec92627aa898a |
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| Source note | uspto-grants-2003_08 |
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