CAS: 1505-50-6; 3-(P-Tolyl)Propionic Acid

该化合物是一种芳香的碳酸,其特点是其丙基酸脊椎被一个准甲基苯基组所取代,其特点是一种芳香的碳酸;该化合物一般是白色的脱白晶体固态,可溶于乙醇和丙酮等有机溶剂,但水中的溶解性有限;其分子结构具有一种传播酸性能的丙酸功能组(-COOH),能够参与各种化学反应,包括酯化和恐吓;该亚甲基苯基体组的存在有助于其防水特性,并影响其与生物系统的再活动与互动;该化合物对有机合成具有兴趣,可作为生产药品和农用化学品的一种中间体;此外,其在研究和工业中的潜在应用突出了解其化学行为和特性的重要性;应参考安全数据处理和储存,如同任何化学物质一样.

结构式图片

相似化合物

5406-39-3 501-52-0 58420-21-6

欧盟法规

ECHA物质C&L通报REACH预注册

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合成工艺路线路线简述

    4-Methylcinnamic Acid置于palladium On Activated Charcoal 氢气体系中,用 乙酸乙酯 用作溶剂,以92%的收率获得3-(4-甲苯)丙酸
    参考文献:原位生成的二恶英酮对苯酚和茴香的区域选择性分子内氧化
    标题:原位生成的二恶英酮对苯酚和茴香的区域选择性分子内氧化
    摘要:已经开发了一种用于酚和茴香的区域选择性氧化的新方法,其中由酮和oxone原位生成的二恶英类化合物以分子内方式氧化酚衍生物.一系列具有吸电子基团的酮,例如cf(3),Coome和ch(2)cl,通过c(2)或c(3)亚甲基连接基连接到苯酚,茴香醚或芳基环上.在ch(3)cn和h(2)o的均相溶剂系统中,苯酚衍生物1-10的氧化反应以2-55%的收率获得螺2-羟基二烯酮,而与其他取代基的存在无关(邻位me,间位me或br)和芳基环的长度.提供了实验证据来支持涉及芳基环的区域选择性pi键环氧化,然后环氧化物重排和半缩酮形成的机制.
    Doi:10.1021/jo000458J

    海关参考信息

    专利信息


    专利号:US-4544450-A
    优先权日:1980-07-15
    标 题 :Electrochemical process for the synthesis of organic compounds
    发明人:OBERRAUCH ERMANNO; EBERSON LENNARD
    权利人:ANIC SPA
    摘要:An electrochemical process is disclosed for the synthesis of organic compounds, said process having the unique characteristic that the element evolved at the anode is exploited by having it reacting with the product of electrolysis obtained at the cathode by the presence of an appropriate catalyst. The catalyst may be associated in the most convenient manner to the anode, or it can be the anode itself. The process opens the way to a number of synthesis reaction which may be carried out electrolytically instead of the conventional ways.

    专利号:US-5329022-A
    优先权日:1991-01-16
    标 题:Process for the synthesis of citraconimides
    发明人:TALMA AUKE G; HOOFT HENDRIKA P M; VAN DE BOVENKAMP-BOUWMAN ANNA
    权利人:AKZO AMERICA INC
    摘要:The present invention relates to an improved synthesis method for the making of citraconimides wherein a citraconic anhydride is reacted with 0.5 to 2.0 equivalents of at least one amine salt. This process may be carried out in a solvent and generally leads to excellent yields of the citraconimides with high selectivity and easy purification. The present inventional so relates to a process for the production of citraconic anhydride from itaconic anhydride with an amine or phosphine catalyst and in a cosolvent.

    专利号:US-9802952-B2
    优先权日:2013-07-15
    标 题:Method and apparatus for the synthesis of dihydroartemisinin and artemisinin derivatives
    发明人:KOPETZKI DANIEL; MCQUADE DAVID TYLER; SEEBERGER PETER H; GILMORE KERRY
    权利人:MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WSS E V; MAX-PLANK-GESELLSCHAFT ZUR FÖRDERUNG DER WSS E V
    摘要:The present invention is directed to a method for continuous production of dihydroartemisinin and also artemisinin derivatives derived from dihydroartemisinin by using artemisinin or dihydroartemisinic acid (DHAA) as starting material as well as to a continuous flow reactor for producing dihydroartemisinin as well as the artemisinin derivatives. It was found that the reduction of artemisinin to dihydroartemisinin in a continuous process requires a special kind of reactor and a special combination of reagents comprising a hydride reducing agent, at least one activator such as an inorganic activator, at least one solid base, at least one aprotic solvent and at least one C 1 -C 5 alcohol.

    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

    专利号:US-6531470-B1
    优先权日:1998-01-23
    标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
    发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
    权利人:UPJOHN CO
    摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.

    专利号:EP-3515880-B1
    优先权日:2017-03-17
    标题:Methods and compositions for synthesis of encoded libraries
    发明人:LI JIN; MORGAN BARRY A; Wan jinqiao; DOU DENGFENG; LIU GUANSAI; CHANG YONG; CHEN QIUXIA; WANG XING; XU YANSHAN; HU DONGYAN; LIU JIAN; CHENG XUEMIN
    权利人:HITGEN INC
    海盐县精细化工有限公司
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    主要参考文献

    [参考文献]: Gregory H Merriman, Et Al. Synthesis And Sar Of Novel 4,5-Diarylimidazolines As Potent P2X7 Receptor Antagonists. Bioorg Med Chem Lett. 2005 Jan 17;15(2):435-8.

    合成参考文献


    摘要:Merino, P., Science of Synthesis, (2010) 45, 289.
    摘要:E. N. Trachtenberg and G. Odian, J. Am. Chem. Soc. 80, 4018 (1958).
    摘要:Sawamura, M.; Shimizu, Y., Science of Synthesis: Knowledge Updates, (2024) 2, 214.
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