1',3-二甲基-5H-螺[呋喃-2,3'-吲哚]-2'(1'H)-酮 | 870152-14-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 1',3-二甲基-5H-螺[呋喃-2,3'-吲哚]-2'(1'H)-酮
• 英文名称: 1',3-dimethyl-5H-spiro[furan-2,3'-indolin]-2'-one
• 英文别名: 1',3-Dimethyl-spiro[furan-2(5H),3'-[3H]indol]-2'(1'H)-one；1',4-dimethylspiro[2H-furan-5,3'-indole]-2'-one
• CAS: 870152-14-0
• 化学式: C₁₃H₁₃NO₂
• 分子量: 215.252
• InChiKey: AIUWZNLCPNUBDU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  29.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1',3-二甲基-5H-螺[呋喃-2,3'-吲哚]-2'(1'H)-酮 在 gold(III) chloride 、 N-溴代丁二酰亚胺(NBS) 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以95%的产率得到5'-bromo-1',4-dimethylspiro[2H-furan-5,3'-indole]-2'-one
  参考文献：
  名称：

  Metal-catalyzed rearrangements of 3-allenyl 3-hydroxyindolin-2-ones in the presence of halogenated reagents

  摘要：

  研究人员探讨了 3-烯基 3-羟基吲哚与多种卤代试剂在催化量贵金属盐存在下的反应。重排反应和氧环化反应分别生成 4-（1-卤乙烯基）-喹啉二酮或螺环卤代吲哚，这两种反应都是竞争性途径。官能化的种类取决于底物和反应条件。

  DOI：

  10.1039/c2ob27359d
• 作为产物：
  描述：

  3-hydroxy-1-methyl-3-(1-methyl-propa-1,2-dienyl)-1,3-dihydro-indol-2-one 在 gold(III) chloride 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以98%的产率得到1',3-二甲基-5H-螺[呋喃-2,3'-吲哚]-2'(1'H)-酮
  参考文献：
  名称：

  Metal-catalyzed rearrangements of 3-allenyl 3-hydroxyindolin-2-ones in the presence of halogenated reagents

  摘要：

  研究人员探讨了 3-烯基 3-羟基吲哚与多种卤代试剂在催化量贵金属盐存在下的反应。重排反应和氧环化反应分别生成 4-（1-卤乙烯基）-喹啉二酮或螺环卤代吲哚，这两种反应都是竞争性途径。官能化的种类取决于底物和反应条件。

  DOI：

  10.1039/c2ob27359d

文献信息

• Palladium Nanoparticles in Water: A Reusable Catalytic System for the Cycloetherification or Benzannulation of α-Allenols
  作者：Benito Alcaide、Pedro Almendros、Ana M. González、Amparo Luna、Sagrario Martínez-Ramírez

  DOI：10.1002/adsc.201501132

  日期：2016.6.16

  A convenient ligand‐free catalytic system has been developed for the chemoselective cyclization reaction of various α‐allenol derivatives by palladium nanoparticles (PdNPs) in an aqueous reaction medium.

  已经开发了一种便捷的无配体催化体系，用于在水性反应介质中通过钯纳米粒子（PdNP）对各种α-烯醇衍生物进行化学选择性环化反应。
• Pd-Cu Bimetallic Catalyzed Domino Cyclization of α-Allenols Followed by a Coupling Reaction: New Sequence Leading to Functionalized Spirolactams
  作者：Benito Alcaide、Pedro Almendros、Raquel Rodríguez-Acebes

  DOI：10.1002/chem.200500228

  日期：2005.9.19

  A novel regioselective metal-catalyzed spirocyclization of alpha-allenols-cross coupling (Heck, Sonogashira, and Suzuki) reaction sequence, leading to potentially bioactive spirocyclic lactam derivatives has been developed. Precursors for the tandem spirocyclization-coupling reaction, alpha-allenols 2 a-d were obtained starting from alpha-oxolactams 1 a-c via indium-mediated Barbier-type carbonyl-allenylation

  已经开发出新颖的区域选择性金属催化的α-烯醇-交叉偶联（Heck，Sonogashira和Suzuki）反应序列的螺环化，从而导致潜在的生物活性螺环内酰胺衍生物。使用我们之前描述的方法，在水性介质中，通过铟介导的Barbier型羰基-烯基化反应，从α-氧代内酰胺1 ac开始，进行串联螺环化偶联反应的前体α-allenols2 ad。
• An Alternative to Precious Metals: Hg(ClO₄)₂·3H₂O as a Cheap and Water-Tolerant Catalyst for the Cycloisomerization of Allenols
  作者：Benito Alcaide、Pedro Almendros、Amparo Luna、Elena Soriano

  DOI：10.1021/acs.joc.5b00887

  日期：2015.7.17

  Hg(ClO4)(2)center dot 3H(2)O, a cheap, water-tolerant, and stable salt, catalyzes the cydoisomerization reaction or alpha-allenols to 2,5-dihydrofurans in an efficient and selective manner. The reaction is general and can be applied to differently functionalized substrates, including alkyl-substituted, aryl-substituted, enantiopure, and tertiary allenols. In addition, density functional theory (DFT) calculations were performed to obtain insight into various aspects of the controlled reactivity of a-allenols under mercury catalysis. They suggest a dual activation of the allenol by the Hg complex that drives the reaction to the chemoselective formation of 2,5-dihydrofurans.
• Efficient Entry to Diversely Functionalized Spirocyclic Oxindoles from Isatins through Carbonyl-Addition/Cyclization Reaction Sequences
  作者：Benito Alcaide、Pedro Almendros、Raquel Rodríguez-Acebes

  DOI：10.1021/jo0525027

  日期：2006.3.1

  A novel approach to diversely functionalized spirocyclic oxindoles has been developed by using different metal-mediated carbonyl-addition/cyclization reaction sequences. Spirocyclization precursors, 2-indolinonetethered homoallylic alcohols, (buta-1,3-dien-2-yl)methanols, and alpha-allenols have been obtained by regioselective addition of stabilized organoindium reagents to isatins in aqueous environment. Ruthenium-, silver-, and palladium-catalyzed reactions of the above unsaturated alcohol derivatives provided oxaspiro oxindoles.
• Gallium-Catalyzed Domino Arylation/Oxycyclization of Allenes with Phenols
  作者：Benito Alcaide、Pedro Almendros、Fernando Herrera、Amparo Luna、M. Elena de Orbe、M. Rosario Torres

  DOI：10.1021/acs.joc.5b00106

  日期：2015.4.17

  The synthesis of dihydrobenzofuran-appended oxindoles has been accomplished taking advantage of an unprecedented reaction between allenols and phenols under metal catalysis.