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HRID 275484생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/275484

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
반응물1-(4-(Methylthio)phenyl)ethan-1-oneHCID 74501—
용매AcetonitrileHCID 6342—
생성물1-Methylthio-4-[1[(trimethylsilyl)oxy]ethenyl]benzeneHCID 10014461101.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393790
출처 데이터셋uspto-grants-1995_02
ORD IDord-34a561d356c84a0883c4bf96aeea64a1
출처 메모uspto-grants-1995_02