6-Cyclopropylfulvene | 129379-51-7

• 分子结构分类: 有机化合物 - 碳氢化合物 - 不饱和烃
• 英文名称: 6-Cyclopropylfulvene
• 英文别名: 5-(Cyclopropylmethylidene)cyclopenta-1,3-diene
• CAS: 129379-51-7
• 化学式: C₉H₁₀
• 分子量: 118.178
• InChiKey: LCHGTJIGVPEFQS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  6-Cyclopropylfulvene 、 对苯醌 以 水 为溶剂， 反应 12.0h， 生成 (1S,4R,4aR,8aS)-9-[1-Cyclopropyl-meth-(Z)-ylidene]-1,4,4a,8a-tetrahydro-1,4-methano-naphthalene-5,8-dione
  参考文献：
  名称：

  Synthese von 7-Alkyliden-tricyclo[6.3.0.02,6]undeca-4,9-dien-3,11-dionen

  摘要：

  The cycloaddition reaction of 6-alkyl- as well as 6,6-dialkyl substituted pentafulvenes 1a - f with 1,4-benzoquinone proceeded efficiently and highly endo-stereoselectively when water was used as the solvent. The adducts 2a - f easily underwent intramolecular photocycloaddition when irradiated in acetone or cyclohexane. The resulting trishomocubanediones 3a - f could be transformed into linearly fused tricyclopentanoids 4a - f via flash vacuum thermolysis.

  DOI：

  10.1002/prac.19923340703
• 作为产物：
  描述：

  4-氯丁醛 、 环戊二烯 在 四氢吡咯 作用下， 以74%的产率得到6-Cyclopropylfulvene
  参考文献：
  名称：

  Scope and Limitations of Fulvene Syntheses. Preparation of 6-Vinyl-Substituted and -Functionalized Fulvenes. First Examples of Nucleophilic Substitution on a 6-(Chloromethyl)fulvene

  摘要：

  Very few 6-vinylfulvenes have previously been reported in the Literature. In a few cases where Little's procedure (using pyrrolidine as base) has been employed, most enones undergo conjugate attack by the cyclopentadienyl anion followed by either a retroaldol reaction or dihydropentalene formation. In several cases, Diels-Alder reaction of the enone with cyclopentadiene occurs rather than condensation. We have found that in cases where the Little procedure fails to give the desired 6-vinylfulvenes, the Thiele method using NaOH (or NaOMe in some cases) as base gives satisfactory results. In the latter instances, Michael attack is completely suppressed in all but one example. By appropriate choice of base, a variety of fulvenes carrying functional groups on the 6-alkyl position can be prepared. Some of these fulvenes have been shown to undergo further functional group transformations (e.g., nucleophilic substitutions); giving rise to derivatives bearing SR, S(O)R, N-3 or SCN groups.

  DOI：

  10.1021/jo00109a010

文献信息

• Scope and Limitations of Fulvene Syntheses. Preparation of 6-Vinyl-Substituted and -Functionalized Fulvenes. First Examples of Nucleophilic Substitution on a 6-(Chloromethyl)fulvene
  作者：Ihsan Erden、Fu-Pei Xu、Aladin Sadoun、Wyatt Smith、Greg Sheff、Madeleine Ossun

  DOI：10.1021/jo00109a010

  日期：1995.2

  Very few 6-vinylfulvenes have previously been reported in the Literature. In a few cases where Little's procedure (using pyrrolidine as base) has been employed, most enones undergo conjugate attack by the cyclopentadienyl anion followed by either a retroaldol reaction or dihydropentalene formation. In several cases, Diels-Alder reaction of the enone with cyclopentadiene occurs rather than condensation. We have found that in cases where the Little procedure fails to give the desired 6-vinylfulvenes, the Thiele method using NaOH (or NaOMe in some cases) as base gives satisfactory results. In the latter instances, Michael attack is completely suppressed in all but one example. By appropriate choice of base, a variety of fulvenes carrying functional groups on the 6-alkyl position can be prepared. Some of these fulvenes have been shown to undergo further functional group transformations (e.g., nucleophilic substitutions); giving rise to derivatives bearing SR, S(O)R, N-3 or SCN groups.
• Synthese von 7-Alkyliden-tricyclo[6.3.0.02,6]undeca-4,9-dien-3,11-dionen
  作者：Axel G. Griesbeck

  DOI：10.1002/prac.19923340703

  日期：——

  The cycloaddition reaction of 6-alkyl- as well as 6,6-dialkyl substituted pentafulvenes 1a - f with 1,4-benzoquinone proceeded efficiently and highly endo-stereoselectively when water was used as the solvent. The adducts 2a - f easily underwent intramolecular photocycloaddition when irradiated in acetone or cyclohexane. The resulting trishomocubanediones 3a - f could be transformed into linearly fused tricyclopentanoids 4a - f via flash vacuum thermolysis.