6-Cyclopropyl-6-methyl-6,7-dihydro-3H-indene-4,4,5,5-tetracarbonitrile | 133744-78-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚和异茚
• 英文名称: 6-Cyclopropyl-6-methyl-6,7-dihydro-3H-indene-4,4,5,5-tetracarbonitrile
• 英文别名: 6-Cyclopropyl-6-methyl-3,7-dihydroindene-4,4,5,5-tetracarbonitrile
• CAS: 133744-78-2
• 化学式: C₁₇H₁₄N₄
• 分子量: 274.325
• InChiKey: KAPNSPSGCHOCNW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  21
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  95.2
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  2'-cyclopropyl-2'-methylspiro[bicyclo[2.2.1]hept-5-ene-7,1'-cyclopropane]-2,2,3,3-tetracarbonitrile 、 乙腈 生成 6-Cyclopropyl-6-methyl-6,7-dihydro-3H-indene-4,4,5,5-tetracarbonitrile
  参考文献：
  名称：

  NISHIDA, SHINYA;ASANUMA, NAOKI;TSUJI, TAKASHI;IMAI, TOSHIRO, CHEM. LETT.,(1991) N, C. 495-498

  摘要：

  DOI：

文献信息

• Reactions of spiro[2.4]hept-4-ene derivatives with tetracyanoethylene. Extensive rearrangements involving aza-Cope process
  作者：Shinya Nishida、Naoki Asanuma、Masashi Murakami、Takashi Tsuji、Toshiro Imai

  DOI：10.1021/jo00043a024

  日期：1992.8

  In CH2Cl2 or CH3CN, 1,1-dicyclopropylspiro[2.4]hept-4-ene (4a) reacted readily with TCNE in a unique to give 4-[N-(dicyclopropylmethylene)amino]-6-methylenebicyclo[3.3.0]oct-3-ene-2,2,3-tricarbonitrile (8a), an imine after extensive rearrangements, and 3,3-dicyclopropylspiro[4.4]non-6-ene-1,1,2,2-tetracarbonitrile (9a), a [sigma-2 + pi-2] cycloadduct. In the reaction of 1-cyclopropyl-1-methyl derivative 4b, 3-(1,1,2,2-tetracyanoethyl)-1-(2-cyclopropylallyl)cyclopentene (10a), formally a vinylogous homoene type adduct, was also produced in addition to 8b and 9b. The reaction of 1,1-dimethyl derivative 4c produced 10b, exclusively. The reaction of 1,1-dicyclopropylbenzo[f]spiro[2.4]hept-4-ene (5a) gave exclusively imine 11, a benzoanalog of 8a, whereas the reaction of saturated benzo derivatives 7 produced 15, corresponding to 9. The production of 8 (as well as 11) and 10 might be depicted in a stepwise dipolar fashion, in which the first formed intermediate 17 will open its spiro-linked three-membered ring to give the second zwitterion 18, which then either cyclizes to a nine-membered adduct 19 or undergoes a proton transfer to give 20. 19 then undergoes aza-Cope rearrangement to afford 8, and 20 ultimately tautomerizes to 10. The parent spiroheptene 4d gave merely a mixture of [pi-2 + pi-2] cycloadduct 14 and [sigma-2 + pi-2] cycloadduct 9c. The formation of 8 and/or 10 is thus limited to occur in such vinylcyclopropanes that hold suitable pendant substituents which can provide greater stabilization to the zwitterionic intermediates. Even in the reaction of spiro[2.4]hepta-4,6-dienes with TCNE, 1,1-dicyclopropyl derivative 2a produced a sizable amount of 3a, corresponding to 8, as well as 16a-16a' in addition to the expected [pi-4 + pi-2] cycloadduct 1a, whereas 2b-2c produced simply the corresponding Diels-Alder adduct.
• Nishida, Shinya; Asanuma, Naoki; Tsuji, Takashi, Chemistry Letters, 1991, # 3, p. 495 - 498
  作者：Nishida, Shinya、Asanuma, Naoki、Tsuji, Takashi、Imai, Toshiro

  DOI：——

  日期：——
• NISHIDA, SHINYA;ASANUMA, NAOKI;TSUJI, TAKASHI;IMAI, TOSHIRO, CHEM. LETT.,(1991) N, C. 495-498
  作者：NISHIDA, SHINYA、ASANUMA, NAOKI、TSUJI, TAKASHI、IMAI, TOSHIRO

  DOI：——

  日期：——