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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6964Generated: October 28, 2026

Chlorotrimethylsilane → 2-Trimethylsilyl-3-methylsulfanylthiophene

https://huagongshe.com/reaction/6964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-(Methylthio)thiopheneHCID 519806—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-Trimethylsilyl-3-methylsulfanylthiopheneHCID 2201946948%

Reaction Conditions

Temperature-70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084170B2
Source datasetuspto-grants-2006_08
ORD IDord-9191d766b42f4cd196abeaea614de401
Source noteuspto-grants-2006_08