戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 275484作成日:2026年10月25日

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

https://huagongshe.com/reaction/275484

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—
溶媒AcetonitrileHCID 6342—
生成物1-Methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzeneHCID 10014461101.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05393790
出典データセットuspto-grants-1995_02
ORD IDord-34a561d356c84a0883c4bf96aeea64a1
出典メモuspto-grants-1995_02