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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1-(4-(Methylthio)phenyl)ethan-1-one | HCID 74501 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-Methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzene | HCID 10014461 | 101,4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05393790 |
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| Quelldatensatz | uspto-grants-1995_02 |
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| ORD ID | ord-34a561d356c84a0883c4bf96aeea64a1 |
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| Quellennotiz | uspto-grants-1995_02 |
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