4-碘苯胺
外觀
4-碘苯胺 | |
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識別 | |
CAS號 | 540-37-4 |
SMILES |
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性質 | |
化學式 | C6H6IN |
摩爾質量 | 219.02 g·mol−1 |
熔點 | 66 °C(339 K)[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
4-碘苯胺是一種有機化合物,化學式為C6H6IN,它是三種碘苯胺的同分異構體之一。它可由4-硝基碘苯被氫氣、硼氫化鈉等還原劑還原得到。[2][3]它和苯甲醛在乙醇中反應,可以得到N-亞苄基-4-碘苯胺。[4]在鈀催化下、碳酸鉀存在下,它和苯硼酸發生偶聯反應,可以得到4-氨基聯苯。[5]
參考文獻
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- ^ Wenjun Yu, Lan-Lan Lou, Shanshan Li, Tianyuan Ma, Lezi Ouyang, Li Feng, Shuangxi Liu. Highly efficient and durable platinum nanocatalysts stabilized by thiol-terminated poly(N-isopropyl acrylomide) for selective hydrogenation of halonitrobenzene to haloaniline. RSC Advances. 2017, 7 (2): 751–757 [2021-11-15]. ISSN 2046-2069. doi:10.1039/C6RA24773C (英語).
- ^ Sanya Pachisia, Ram Kishan, Samanta Yadav, Rajeev Gupta. Half-Sandwich Ruthenium Complexes of Amide-Phosphine Based Ligands: H-Bonding Cavity Assisted Binding and Reduction of Nitro-substrates. Inorganic Chemistry. 2021-02-01, 60 (3): 2009–2022 [2021-11-15]. ISSN 0020-1669. doi:10.1021/acs.inorgchem.0c03505. (原始內容存檔於2021-11-01) (英語).
- ^ Romero, Eugenie; Oueslati, Saoussen; Benchekroun, Mohamed; D'Hollander, Agathe C. A.; Ventre, Sandrine; Vijayakumar, Kamsana; Minard, Corinne; Exilie, Cynthia; Tlili, Linda; Retailleau, Pascal; Zavala, Agustin; Elisee, Eddy; Selwa, Edithe; Nguyen, Laetitia A.; Pruvost, Alain; Naas, Thierry; Iorga, Bogdan I.; Dodd, Robert H.; Cariou, Kevin. Azetidinimines as a novel series of non-covalent broad-spectrum inhibitors of β-lactamases with submicromolar activities against carbapenemases of classes A, B and D. ChemRxiv, 2020. 1-31.
- ^ Hongxue Xie, Huihui Liu, Meimei Wang, Hui Pan, Caixia Gao. L‐Tyrosine‐Pd complex supported on Fe 3 O 4 magnetic nanoparticles: A new catalyst for C–C coupling and Synthesis of sulfides. Applied Organometallic Chemistry. 2020-01, 34 (1) [2021-11-15]. ISSN 0268-2605. doi:10.1002/aoc.5256. (原始內容存檔於2021-11-15) (英語).