聯苯-4-甲酸
聯苯-4-甲酸 | |
---|---|
識別 | |
CAS號 | 92-92-2 |
性質 | |
化學式 | C13H10O2 |
摩爾質量 | 198.22 g·mol−1 |
外觀 | 白色固體[1] |
熔點 | 228—230 °C(501—503 K)[1] |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
聯苯-4-甲酸是一種有機化合物,化學式為C13H10O2,它是三種聯苯甲酸的同分異構體之一。它可由4-溴苯甲酸和苯硼酸在碳酸鉀存在下、鈀催化下偶聯,生成物酸化後得到;在鈀中引入金可以阻止催化劑滲出。[2]在DMF催化下,它和氯化亞碸[3]或草醯氯[4]反應,可以得到聯苯-4-甲醯氯。在氟化鈉存在下,它和N,N-二乙基二氟硫亞銨氟硼酸鹽反應,可以得到聯苯-4-甲醯氟。[5]
參考文獻
- ^ 1.0 1.1 Zhengyin Du, Wanwei Zhou, Fen Wang, Jin-Xian Wang. In situ generation of palladium nanoparticles: ligand-free palladium catalyzed ultrafast Suzuki–Miyaura cross-coupling reaction in aqueous phase at room temperature. Tetrahedron. 2011-07, 67 (26): 4914–4918 [2022-10-19]. doi:10.1016/j.tet.2011.04.093. (原始內容存檔於2022-06-19) (英語).
- ^ Raghu Nath Dhital, Karan Bobuatong, Masahiro Ehara, Hidehiro Sakurai. Gold/Palladium Alloy for Carbon-Halogen Bond Activation: An Unprecedented Halide Dependence. Chemistry - An Asian Journal. 2015-12, 10 (12): 2669–2676 [2022-10-19]. doi:10.1002/asia.201500722. (原始內容存檔於2022-10-19) (英語).
- ^ Dongxu Zuo, Qun Wang, Long Liu, Tianzeng Huang, Michal Szostak, Tieqiao Chen. Highly Chemoselective Transamidation of Unactivated Tertiary Amides by Electrophilic N−C(O) Activation by Amide‐to‐Acyl Iodide Re‐routing. Angewandte Chemie International Edition. 2022-06-13, 61 (24) [2022-10-19]. ISSN 1433-7851. doi:10.1002/anie.202202794. (原始內容存檔於2022-10-19) (英語).
- ^ Md Emdadul Hoque, Mirja Md Mahamudul Hassan, Buddhadeb Chattopadhyay. Remarkably Efficient Iridium Catalysts for Directed C(sp 2 )–H and C(sp 3 )–H Borylation of Diverse Classes of Substrates. Journal of the American Chemical Society. 2021-04-07, 143 (13): 5022–5037 [2022-10-19]. ISSN 0002-7863. doi:10.1021/jacs.0c13415. (原始內容存檔於2022-10-19) (英語).
- ^ Marie Gonay, Chloé Batisse, Jean-François Paquin. Synthesis of Acyl Fluorides from Carboxylic Acids Using NaF-Assisted Deoxofluorination with XtalFluor-E. The Journal of Organic Chemistry. 2020-08-07, 85 (15): 10253–10260 [2022-10-19]. ISSN 0022-3263. doi:10.1021/acs.joc.0c01377. (原始內容存檔於2022-10-21) (英語).