化学
亲核芳香族取代
分子内力
芳基
药物化学
光化学
有机化学
亲核取代
烷基
作者
Takashi Shigeta,Yoshiyasu Ichikawa,Shiho Suzuki,Yui Hamabe,Nobuo Nakahara,Yuka Gonno,Minoru Ozeki,Ikuo Kawasaki,Masahiro Egi
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2024-11-28
卷期号:57 (04): 883-890
摘要
Abstract N-(Trimethylsilyl)diethylamine (TMSNEt2) significantly promotes intramolecular nucleophilic aromatic substitution (SNAr) reactions of electron-rich aryl fluorides with t-BuOK and crown ether. Although substrates bearing electron-donating groups are conventionally inert under SNAr conditions, the activation of substrates by TMSNEt2 enables the reactions to proceed even at room temperature. This method is applicable to the preparation of benzo-fused oxygen-containing heterocycles, such as 3,4-dihydro-2H-1,4-benzoxazines, 3,4-dihydro-2H-1,5-benzoxazepines, and 3,4-dihydro-2H-1-benzopyran, in good to excellent yields (56–93%).
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