4-异丙基-3,4-二甲基-2-环戊烯-1-酮 | 131794-49-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 4-异丙基-3,4-二甲基-2-环戊烯-1-酮
• 英文名称: 4-(1-Methylethyl)-3,4-dimethyl-2-cyclopentenone
• 英文别名: 3,4-Dimethyl-4-propan-2-ylcyclopent-2-en-1-one
• CAS: 131794-49-5
• 化学式: C₁₀H₁₆O
• 分子量: 152.236
• InChiKey: FPTLWNPHWWQJTB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  (E)-2,7-dimethyl-4-oxo-2,5-octadiene 在 硫酸 作用下， 以31%的产率得到4-异丙基-3,4-二甲基-2-环戊烯-1-酮
  参考文献：
  名称：

  Nazarov reaction of trisubstituted dienones: mechanism involving Wagner-Meerwein shift

  摘要：

  The Nazarov reactions of trisubstituted alpha,alpha'-dienones were studied. Whereas alpha,beta-dimethyl-beta'-alkyl alpha,alpha'-dienones gave 2,3-dimethyl-4-alkyl-2-cyclopentenones when heated in concentrated sulfuric acid, the reaction of beta,beta-dimethyl-beta'-alkyl alpha,alpha'-dienones afforded 3,4-dimethyl-4-alkyl-2-cyclopentenones as the rearranged products. A mechanistic investigation using two deuterated dienones suggests that the Nazarov reactions of the latter dienones are accompanied by Wagner-Meerwein shifts to form the most stable carbocations.

  DOI：

  10.1021/jo00002a047

文献信息

• MOTOYOSHIYA, JIRO;YAZAKI, TOSHIKAZU;HAYASHI, SADAO, J. ORG. CHEM., 56,(1991) N, C. 735-740
  作者：MOTOYOSHIYA, JIRO、YAZAKI, TOSHIKAZU、HAYASHI, SADAO

  DOI：——

  日期：——
• Nazarov reaction of trisubstituted dienones: mechanism involving Wagner-Meerwein shift
  作者：Jiro Motoyoshiya、Toshikazu Yazaki、Sadao Hayashi

  DOI：10.1021/jo00002a047

  日期：1991.1

  The Nazarov reactions of trisubstituted alpha,alpha'-dienones were studied. Whereas alpha,beta-dimethyl-beta'-alkyl alpha,alpha'-dienones gave 2,3-dimethyl-4-alkyl-2-cyclopentenones when heated in concentrated sulfuric acid, the reaction of beta,beta-dimethyl-beta'-alkyl alpha,alpha'-dienones afforded 3,4-dimethyl-4-alkyl-2-cyclopentenones as the rearranged products. A mechanistic investigation using two deuterated dienones suggests that the Nazarov reactions of the latter dienones are accompanied by Wagner-Meerwein shifts to form the most stable carbocations.