4-碘吡啶
4-碘吡啶 | |
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英文名 | 4-iodopyridine |
識別 | |
CAS號 | 15854-87-2 ![]() |
性質 | |
化學式 | C5H4IN |
摩爾質量 | 205 g·mol−1 |
熔點 | 106—108 °C(379—381 K)[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
4-碘吡啶是一種有機化合物,化學式為C5H4IN,是碘吡啶的同分異構體之一。它可由4-氨基吡啶反應得到重氮鹽後與碘化鉀反應得到。[2]4-氯吡啶鹽酸鹽和碘化鈉在乙腈中反應也可以得到4-碘吡啶。[3]它和芳基硼酸在四(三苯基膦)鈀的催化下反應,可以得到4-吡啶基芳基化合物。[4]
參考文獻
- ^ Yasuyuki Suzuki. Synthesis of 4-Iodopyridine and its Homologs. YAKUGAKU ZASSHI. 1961, 81 (8): 1206–1207 [2020-05-29]. ISSN 0031-6903. doi:10.1248/yakushi1947.81.8_1206. (原始內容存檔於2018-06-01) (英語).
- ^ C. Coudret. Efficient Syntheses of 4-Iodopyridine and of 4-Pyridylboronic Acid Pinacol Ester. Synthetic Communications. 1996-10, 26 (19): 3543–3547 [2020-05-29]. ISSN 0039-7911. doi:10.1080/00397919608003763 (英語).
- ^ Pia Bonakdarzadeh, Filip Topić, Elina Kalenius, Sandip Bhowmik, Sota Sato, Michael Groessl, Richard Knochenmuss, Kari Rissanen. DOSY NMR, X-ray Structural and Ion-Mobility Mass Spectrometric Studies on Electron-Deficient and Electron-Rich M 6 L 4 Coordination Cages. Inorganic Chemistry. 2015-06-15, 54 (12): 6055–6061 [2020-05-29]. ISSN 0020-1669. doi:10.1021/acs.inorgchem.5b01082 (英語).
- ^ Andrea Czompa, Balázs László Pásztor, Jennifer Alizadeh Sahar, Zoltán Mucsi, Dóra Bogdán, Krisztina Ludányi, Zoltán Varga, István M. Mándity. Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki–Miyaura reaction. RSC Advances. 2019, 9 (65): 37818–37824 [2020-05-29]. ISSN 2046-2069. doi:10.1039/C9RA07044C (英語).