(3-ethyl-1-methyl-2-oxoindolin-3-yl)methyl acetate | 1582285-66-2

• 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
• 英文名称: (3-ethyl-1-methyl-2-oxoindolin-3-yl)methyl acetate
• 英文别名: (3-Ethyl-1-methyl-2-oxoindol-3-yl)methyl acetate
• CAS: 1582285-66-2
• 化学式: C₁₄H₁₇NO₃
• 分子量: 247.294
• InChiKey: VWKIZWHUYBDSPK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  过氧化二异丙苯 、 2-(methyl(phenyl)carbamoyl)allyl acetate 在 三乙烯二胺 、 iron(II) acetate 作用下， 以 二甲基亚砜 为溶剂， 反应 12.0h， 以58%的产率得到(3-ethyl-1-methyl-2-oxoindolin-3-yl)methyl acetate
  参考文献：
  名称：

  Iron-Catalyzed Oxidative Arylmethylation of Activated Alkenes Using a Peroxide as the Methyl Source

  摘要：

  A novel, simple route for the synthesis of oxindoles is presented via iron-catalyzed oxidative arylmethylation of activated alkenes with peroxides. This work is realized by the use of a peroxide as the methyl source and 1,4-diazabicyclo[2.2.2]octane as the ligand and represents a new access to oxindoles through an alkene oxidative difunctionalization process.

  DOI：

  10.1055/s-0033-1340665

文献信息

• The carbomethylation of arylacrylamides leading to 3-ethyl-3-substituted indolin-2-one by cascade radical addition/cyclization
  作者：Qiang Dai、Jintao Yu、Yan Jiang、Songjin Guo、Haitao Yang、Jiang Cheng

  DOI：10.1039/c4cc01053a

  日期：——

  An FeCl2-promoted carbomethylation of arylacrylamides by di-tert-butyl peroxide (DTBP) is achieved, leading to 3-ethyl-3-substituted indolin-2-one in high yield. The reaction tolerates a series of functional groups, such as cyano, nitro, ethyloxy carbonyl, bromo, chloro, and trifluoromethyl groups. The radical methylation and arylation of the alkenyl group are involved in this reaction.

  利用二叔丁基过氧化物（DTBP）实现的FeCl2促进的芳基丙烯酰胺的甲酸甲酯化反应，以高产率得到3-乙基-3-取代的吲哚啉-2-酮。该反应容忍一系列官能团，如氰基、硝基、乙氧羰基、溴、氯和三氟甲基等。反应涉及烯丙基的自由基甲基化和芳基化。
• An Iron(II) Chloride-Promoted Radical Cascade Methylation or α-Chloro-β-methylation of<i>N</i>-Arylacrylamides with Dimethyl Sulfoxide
  作者：Zejiang Li、Xiaosong Cui、Lin Niu、Yingming Ren、Menghua Bian、Xuebiao Yang、Biao Yang、Qinqin Yan、Jincan Zhao

  DOI：10.1002/adsc.201601001

  日期：2017.1.19

  A free radical‐initiated methylation and/or α‐chloro‐β‐methylation of N‐arylacrylamides with dimethyl sulfoxide under the analogous Fenton reaction condition has been developed, which provides an effective and facile cascade strategy for the synthesis of oxindoles and chlorinated amides.

  已开发了在类似的Fenton反应条件下，N-芳基丙烯酰胺与二甲基亚砜进行自由基引发的甲基化和/或α-氯-β-甲基化的方法，为合成羟吲哚和氯化酰胺提供了一种有效且简便的级联策略。