HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6964Generated: October 28, 2026
Chlorotrimethylsilane → 2-Trimethylsilyl-3-methylsulfanylthiophene
https://huagongshe.com/reaction/6964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 3-(Methylthio)thiophene | HCID 519806 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Trimethylsilyl-3-methylsulfanylthiophene | HCID 22019469 | 48% |
Reaction Steps
A solution of n-BuLi (5.3 mL of 1.6 M in hexanes, 8.5 mmol) is added dropwise to a solution of 3-methylsulfanylthiophene (1.0 g, 7.7 mmol) in anhydrous Et2O (8 mL) under nitrogen at −70° C. The mixture is stirred at −70° C. for 2 hr. Chlorotrimethylsilane (1.5 mL) is added slowly to the reaction mixture. The mixture is warmed to room temperature and stirred for 3 hr. The reaction is quenched with water (50 mL) and Et2O (50 mL). The aqueous layer is extracted with Et2O (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 (0.75 g, 48%) 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-9191d766b42f4cd196abeaea614de401 |
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| Source note | uspto-grants-2006_08 |
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