CAS: 127-66-2; 2-Phenylbut-3-Yn-2-Ol

该化合物是有机化合物,其特点是其烷功能组和一个氢氧基组;该化合物的特征是附于丁醇结构的一个苯基组,特别是在丁基链的第二个位置;该化合物一般是无色的黄色液体,其芳香味不同;该物质的存在使该物质成为影响其反应性和溶性特性的二次酒精. 2-phenyl-3-butyn-2-ol因其在有机合成中的潜在应用而闻名,特别是在通过核循环哲学替代和组合反应等反应形成更复杂的分子方面.此外,它可能展示有趣的生物活动,使其成为医药化学的一个对象.其稳定性和耐受性可能随温度和催化剂或其他试剂的存在等条件而变化.由于易燃性和毒性的潜在危害,适当的处理和储存是必不可少的.

结构式图片

相似化合物

6712-32-9 159028-51-0 74207-58-2

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合成工艺路线路线简述

    2-苯基-4-(三甲基甲硅烷基)-3-丁炔-2-醇置于potassium Carbonate体系中,用 甲醇 用作溶剂,化学反应 1.0H,反应生成2-苯基-3-丁炔-2-醇
    参考文献:邻羰基辅助的丙炔基羧酸盐的氧乙酰氧基化在无金属条件下保持手性
    标题:邻羰基辅助的丙炔基羧酸盐的氧乙酰氧基化在无金属条件下保持手性
    摘要:提出了保留手性的伯,仲和叔炔丙基羧酸的无金属氧乙酰氧基化方法.该反应通过烷基炔酮中间体上相邻羰基的分子内亲核攻击而进行.该方法是一般的,具有广泛的底物范围,并且适用于包括从天然产物获得的那些炔丙基羧酸酯.通过同位素标记(使用h 2 O 18和d 2 O)洞察机械途径,并确认了对照实验.
    Doi:10.1002/adsc.201900314

    海关参考信息

    专利信息


    专利号:US-7109377-B2
    优先权日:1996-10-16
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
    发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
    权利人:HARVARD COLLEGE
    摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

    专利号:US-5637757-A
    优先权日:1995-04-11
    标 题 :One-pot synthesis of ring-brominated benzoate compounds
    发明人:HILL JOHN E; FAVSTRITSKY NICOLAI A; MAMUZIC RASTKO I; BHATTACHARYA BHABATOSH
    权利人:GREAT LAKES CHEMICAL CORP
    摘要:A method of preparing tetrabromobenzoate compounds from tetrabromophthalic anhydride by reacting tetrabromophthalic anhydride with alcohol in the presence of a decarboxylation catalyst. The reaction may be carried out in an excess of alcohol, or with a near stoichiometric amount of alcohol by performing the reaction in an inert solvent.

    专利号:US-2003082830-A1
    优先权日:1996-10-16
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

    专利号:US-9981923-B2
    优先权日:2014-06-20
    标 题:1,2,3 Triazole antifungal agents and preparation thereof
    发明人:CHEPURI VENKATA RAMANA; DESHPANDE MUKUND VINAYAK; TUPE SANTOSH GENBA; KOMMAGALA YADAGIRI
    权利人:COUNCIL SCIENT IND RES
    摘要:The present application relates to 1,4-disubstituted 1,2,3-Triazole antifungal agents of the formula (I) wherein, R1 is halogens such as fluorine, chlorine or bromine, CF3, alkyl; R2 is alkyl or hydrogen; R3 is halogen selected from fluorine, chlorine or bromine; and n is 0 or 1. The application further relates to the synthesis of said compounds, to fungicidal compositions containing said compounds and to their use in a method for treating fungal infections.

    专利号:WO-0006525-A9
    优先权日:1998-07-25
    标题:Synthesis of combinatorial libraries of compounds reminiscent of natural products

    专利号:WO-0006525-A2
    优先权日:1998-07-25
    标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
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    合成参考文献


    参考文献:10.1007/s00253-011-3464-3
    摘要:Rehdorf J, Behrens GA, Nguyen GS, Kourist R, Bornscheuer UT. Pseudomonas putida esterase contains a GGG(A)X-motif confering activity for the kinetic resolution of tertiary alcohols. Appl Microbiol Biotechnol. 2012 Feb;93(3):1119–26. doi: 10.1007/s00253-011-3464-3.
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