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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275484Erstellt: 24. Oktober 2026

Sodium Iodide → 1-Methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzene

https://huagongshe.com/de/reaction/275484

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktChlorotrimethylsilaneHCID 6397—
EduktTriethylamineHCID 8471—
Edukt1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzeneHCID 10014461101,4%

Reaktionsschritte

Under nitrogen, 11.0 g (66.2 mmol) of 4-(methylthio)acetophenone (prepared in Step 1 of Example 1) and 13.8 mL (99 mmol) of triethylamine in 50 mL of acetonitrile was treated with 12.6 mL (99.3 mmol) of chlorotrimethylsilane at ambient temperature and allowed to stir for 20 minutes prior to the slow addition of a suspension of 14.9 g (99.4 mmol) of sodium iodide in 60 mL of acetonitrile. The reaction was stirred for 3 hours, poured into ice/water, and extracted with hexane. The extracts were combined, dried (K2CO3), and concentrated in vacuo to give 16 g of crude 1-methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzene as an oil: NMR (CDCl3) δ 0.26 (s, 9H), 2.48 (s, 3H), 4.39 (d, J=2 Hz, 1H), 4.87 (d, J=2 Hz, 1H), 7.20 (d, J=8 Hz, 2H), 7.50 (d, J=8Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05393790
Quelldatensatzuspto-grants-1995_02
ORD IDord-34a561d356c84a0883c4bf96aeea64a1
Quellennotizuspto-grants-1995_02