2-(cyclohex-1-en-1-ylethynyl)phenol | 1286764-01-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 2-(cyclohex-1-en-1-ylethynyl)phenol
• 英文别名: 2-[2-(Cyclohexen-1-yl)ethynyl]phenol；2-[2-(cyclohexen-1-yl)ethynyl]phenol
• CAS: 1286764-01-9
• 化学式: C₁₄H₁₄O
• 分子量: 198.265
• InChiKey: DRIMMANNXSSLMX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-(cyclohex-1-en-1-ylethynyl)phenol 在 sodium acetate 、 palladium diacetate 、 potassium carbonate 、 三苯基膦 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 20.5h， 生成 (3-(cyclohex-1-en-1-yl(phenyl)methyl)benzofuran-2-yl)(phenyl)methanone
  参考文献：
  名称：

  通过分子间Carpalpalladation / C（sp3）-H功能化/异构化序列的2,3-二取代苯并呋喃的钯催化多米诺法

  摘要：

  已经开发了钯催化的多米诺骨牌策略来合成2,3-二取代的苯并呋喃衍生物。该级联反应序列涉及分子间碳钯化和C（sp 3）-H官能化，然后是异构化。

  DOI：

  10.1002/adsc.201600356
• 作为产物：
  描述：

  在 盐酸 作用下， 以 四氢呋喃 、 水 、 异丙醇 为溶剂， 反应 16.0h， 生成 2-(cyclohex-1-en-1-ylethynyl)phenol
  参考文献：
  名称：

  Rhodium-Catalyzed Olefin Isomerization/Enantioselective Intramolecular Alder-Ene Reaction Cascade

  摘要：

  The olefin isomerization/enantioselective intramolecular Alder-ene reaction cascade was achieved by using a cationic rhodium(I)/(R)-BINAP complex as a catalyst. A variety of substituted dihydrobenzofurans and dihydronaphthofurans were obtained from phenol- or naphthol-linked 1,7-enynes, respectively, with good yields and ee values.

  DOI：

  10.1021/ol201986e

文献信息

• Efficient microwave-assisted one-pot three-component synthesis of 2,3-disubstituted benzofurans under Sonogashira conditions
  作者：Nataliya A. Markina、Yu Chen、Richard C. Larock

  DOI：10.1016/j.tet.2013.02.003

  日期：2013.4

  efficient one-pot method for the synthesis of 2,3-disubstituted benzo[b]furans from commercially available 2-iodophenols, terminal acetylenes and aryl iodides has been developed utilizing Sonogashira reaction conditions. After an initial Sonogashira coupling of the 2-iodophenol with the terminal alkyne, cyclization involving the aryl iodide provides the 2,3-disubstituted benzo[b]furan in good to excellent

  利用Sonogashira反应条件，已经开发出一种有效的一锅法，由市售的2-碘苯酚，末端乙炔和芳基碘化物合成2,3-二取代的苯并[b]呋喃。在将2-碘苯酚与末端炔烃进行最初的Sonogashira偶联后，涉及芳基碘化物的环化反应可提供2,3-二取代的苯并[b]呋喃，收率非常好。微波辐射的使用缩短了反应时间并使副产物最小化。该方法对于构建高度取代的苯并[b]呋喃及其类似物的库特别有用。
• Indium(III)-Catalyzed Synthesis of Benzo[<i>b</i>]furans by Intramolecular Hydroalkoxylation of <i>ortho</i>-Alkynylphenols: Scope and Mechanistic Insights
  作者：Lorena Alonso-Marañón、M. Montserrat Martínez、Luis A. Sarandeses、Enrique Gómez-Bengoa、José Pérez Sestelo

  DOI：10.1021/acs.joc.8b00829

  日期：2018.8.3

  Indium(III) halides catalyze the hydroalkoxylation reaction of ortho-alkynylphenols to afford benzo[b]furans in good yields. The reaction proceeds with 5-endo-dig regioselectivity with a variety of phenols functionalized at the arene and alkyne moieties in high yields using InI3 (5 mol %) in DCE. Experimental and computational studies support a mechanism based on the indium(III) π-Lewis acid activation

  卤化铟（III）催化邻炔基苯酚的加氢烷氧基化反应，以高收率提供苯并[ b ]呋喃。反应的进行与5-内切-挖区域选择性与各种在芳烃官能酚类和以高产率使用的InI炔基部分3在DCE（5摩尔％）。实验和计算研究支持了基于炔烃的铟（III）π-路易斯酸活化，然后进行苯酚的亲核加成和最终的原金属脱金属，得到相应的苯并[ b ]呋喃的机理。DFT计算表明二聚体In 2 I 6 是通过与炔烃和羟基的新型双配位而催化的物质。
• Gold-Catalyzed Enynal and Enynol Coupling by Selectively Steering Two Transient Vinyl-Gold Intermediates
  作者：Zipeng Wang、Tongxiang Cao、Shifa Zhu

  DOI：10.1021/acs.orglett.2c03890

  日期：2022.12.23

  bond is easily accessible but less exploited in homogeneous gold catalysis, which possesses weak nucleophilicity and would be likely to undergo protodemetalation. Herein, a gold-catalyzed enynal and enynol coupling by selectively steering two transient vinyl-gold intermediates is realized under mild conditions. It exhibits high atom economy and good tolerance of functional groups with the added benefit

  乙烯基-金键很容易获得，但在均相金催化中利用较少，它具有弱亲核性，很可能会发生原脱金属。在此，通过选择性地控制两种瞬态乙烯基金中间体，在温和条件下实现了金催化的烯醛和烯醇偶联。它表现出高原子经济性和官能团的良好耐受性，并具有操作简单的额外好处。对照实验表明，原位形成的乙烯基金是反应性的原因。
• An Annulative Electrophilic Amination Approach to 3-Aminobenzoheteroles
  作者：Naoki Matsuda、Koji Hirano、Tetsuya Satoh、Masahiro Miura

  DOI：10.1021/jo202207s

  日期：2012.1.6

  A copper-catalyzed annulative amination approach to 3-aminobenzofurans and -indoles from o-alkynylphenols and -anilines has been developed. The Cu-based catalysis is based on an umpolung, electrophilic amination with O-benzoyl hydroxylamines and enables the mild and convergent synthesis of various 3-aminobenzoheteroles of biological and pharmaceutical interest. Some mechanistic investigations and an application of this protocol to construction of more complex tricyclic framework are also described.
• Copper-Mediated Annulative Direct Coupling of <i>o</i>-Alkynylphenols with Oxadiazoles: A Dehydrogenative Cascade Construction of Biheteroaryls
  作者：Hitoshi Hachiya、Koji Hirano、Tetsuya Satoh、Masahiro Miura

  DOI：10.1021/ol200975j

  日期：2011.6.17

  A copper-mediated annulative direct coupling of o-alkynylphenols with 1,3,4-oxadiazoles proceeds smoothly even under ambient conditions to afford the corresponding biheteroaryls. The reaction system represents a new avenue for the construction of biheteroaryl molecules of interest in their biological and physical properties.