HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6961Generated: October 26, 2026
Chlorotrimethylsilane → 2-Trimethylsilyl-3-methoxythiophene
https://huagongshe.com/reaction/6961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 3-Methoxythiophene | HCID 140249 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Trimethylsilyl-3-methoxythiophene | HCID 11008640 | 82% |
Reaction Steps
A solution of n-BuLi (19.7 mL of 1.6 M in hexanes, 31.5 mmol) is added dropwise to a solution of 3-methoxythiophene (3.0 g, 26.3 mmol) in anhydrous Et2O (20 mL) under nitrogen at −70° C. The mixture is stirred at −70° C. for 2 hr. Chlorotrimethylsilane (4.5 mL, 35.4 mmol) is added slowly to the solution. The mixture is warmed to room temperature and stirred for 3 hr. The reaction is quenched with water (50 mL) and hexanes (100 mL). The aqueous layer is extracted with hexanes (50 mL). The combined organic extracts are dried (Na2SO4), filtered and concentrated. The crude product is chromatographed on silica gel, eluting with hexanes to afford the title compound (4.0 g, 82%) as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084170B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-565e2ecce6004964ad51bb958a449fdc |
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| Source note | uspto-grants-2006_08 |
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