CAS: 179923-32-1; (2,3,4,5-Tetrafluorophenyl)Boronic Acid

该化合物是一种有机有机体化合物,其特征是,在苯环上有一个含有四氟替代元素的碳酸性功能组,该化合物通常显示白色为白色的离白晶状外表,由于碱酸味,可溶于水和酒精等极地溶剂中,氟酸原子的存在会增强它的再活动性和稳定性,使其在包括有机合成和材料科学在内的各种化学应用中有用.它可以参与铃木-米亚拉的交叉组合反应,这是形成碳-碳联结的关键.此外,氟化结构可能会产生独特的电子特性,使其在制药和农用化学品开发中具有价值.在处理该化合物时,应当考虑到安全因素,因为酸可以是刺激剂,而氟化性质可能构成具体的环境问题.

结构式图片

合成工艺路线路线简述

    📜四氟苯置于正丁基锂,硼酸三异丙酯,盐酸体系中,用 乙醚,正己烷 用作溶剂,化学反应生成2,3,4,5-四氟苯硼酸
    参考文献:(Fluoroorgano)Fluoroboranes And-Fluoroborates I: Synthesis And Spectroscopic Characterization Of Potassium Fluoroaryltrifluoroborates And Fluoroaryldifluoroboranes
    标题:(Fluoroorgano)Fluoroboranes And-Fluoroborates I: Synthesis And Spectroscopic Characterization Of Potassium Fluoroaryltrifluoroborates And Fluoroaryldifluoroboranes
    摘要:A Convenient Preparation Of K[arbf3] (Ar= 2-C6H4F,3-C6H4F,4-C6H4F,2,6-C6H3F2,3,5-C6H3F2,2,4,6-C6H2F3,3,4,5-C6H2F3,2,3,4,5-C6Hf4 And C6F5) Is Offered And The Ir And Multinuclear NMR Spectra Of These Salts Are Reported. Treatment Of The Trifluoroborate Salts With Bf3 In Chlorocarbon Solvents Provides An Easy Synthetic Route To The Corresponding Aryldifluoroboranes Arbf2. The Multinuclear NMR Spectra Of Arbf2 Are Presented. The Electron Substituent Effect Of The [-Bf3](-)-Group Shows This Substituent As One Of The Strongest Sigma-Electron Donors,While Its Pi-Electron Influence Is Negligible (Sigma(I) =-0.32,Sigma(R) =-0.07). (C) 2000 Elsevier Science S.A. All Rights Reserved.
    Doi:10.1016/s0022-328X(99)00690-7

    专利信息


    专利号:US-11225655-B2
    优先权日:2010-04-16
    标题:Bi-functional complexes and methods for making and using such complexes
    发明人:GOULIAEV ALEX HAAHR; FRANCH THOMAS; GODSKESEN MICHAEL ANDERS; JENSEN KIM BIRKEBAEK
    权利人:GOULIAEV ALEX HAAHR; FRANCH THOMAS; GODSKESEN MICHAEL ANDERS; JENSEN KIM BIRKEBAEK; NUEVOLUTION AS
    摘要:The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.

    专利号:WO-2025006693-A1
    优先权日:2023-06-30
    标 题 :Cannabidiol-like compounds and methods for the selective preparation of the same
    发明人:CHITTIBOYINA AMAR G; CHATTERJEE SHAMBA; PANDEY PANKAJ; KHAN IKHLAS A
    权利人:UNIV MISSISSIPPI
    摘要:In one aspect, the disclosure relates to new cannabidiol (CBD) analogs produced from allylic monoterpene alcohols and substituted resorcinols in the presence of aryl boronic acids, efficient and mild synthetic methods of making the new CBD analogs, and improved methods of making known CBD analogs. In one aspect, the methods produce low amounts of tetrahydrocannabinol (THC)-like compounds, low amounts of abnormal cannabidiol (abn-CBD) analogs, and higher amounts of CBD analogs, greatly simplifying purification. The methods can be tailored further to produce low amounts of CBD analogs and higher amounts abn-CBD analogs. In the disclosed methods, synthesis parameters can be varied in order to selectively produce a desired normal or abnormal regioisomer.

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    合成参考文献


    参考文献:10.1055/s-0036-1589040
    摘要:Zheng W, Tang W, Cao K, Meng S. Boronic Acid Catalysis for Aza-Piancatelli Rearrangement. Synthesis. 2017 Jun 20;49(16):3670–5. doi: 10.1055/s-0036-1589040.
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