Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate | 223139-96-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate
• 英文别名: cyclopenta-1,3-diene;[(6Z)-6-(cyclopenta-2,4-dien-1-ylmethylidene)-5-methoxycyclohexa-2,4-dien-1-ylidene]-methyloxidanium;iron(2+);perchlorate
• CAS: 223139-96-6
• 化学式: C₁₉H₁₉FeO₂*ClO₄
• 分子量: 434.656
• InChiKey: JVNASRAZGDINBG-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为反应物：
  描述：

  Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate 在 2-propanol 、 HClO₄ 作用下， 以 异丙醇 为溶剂， 以89%的产率得到Ferrocenyl(2,6-dimethoxyphenyl)methane
  参考文献：
  名称：

  Stability and reactivity of ferrocenyl(2,4,6-trimethoxyphenyl)carbenium salts

  摘要：

  Ferrocenyl(phenyl)methanols, Fc-CH Phi OH [Fc = Fe(eta(5)-C5H5)(eta(5)-C5H4), Phi(a) = 2,4,6-(MeO)(3)C6H2 (1a); Phi(b) = 2,6-(MeO)(2)C6H3 (1b)], were prepared by the reactions of Fc-CHO with Phi Li. 1a reacted with only a slight excess of perchloric acid or tetrafluoroboric acid even in methanol and in 1 M HCl acid to give dark violet crystals of the carbenium salts, [Fc-CH Phi(a)]X [X = ClO4 (2a), BF4 (2a')]. 1b reacted with these acids in diethylether to give the carbenium salts, [Fc-CH Phi(b)]X [X = ClO4 (2b), BF4 (2b') (dark red-brown crystals)] in good yields. The pK(R+) values could be measured in HCl acid for 1a (3.0) and for 1b (1.6). 2a and 2b were labile in hot 2-propanol to give the reduced compounds, Fc-CH(2)Phi. 1a and 1b reacted with 1,3,5-trimethoxybenzene, Phi(a)H, in 2-methyl-2-propanol containing only a slight excess of HCl acid to give diphenyl(ferrocenyl)methanes, Fc-CH Phi(2)(a) and Fc-CH Phi(a)Phi(b), respectively. While 1a decomposed in neat 1,3-dimethoxybenzene, Phi(b)H, in the presence of acid, 1b reacted to give 2,4-dimethoxyphenyl(2,6-dimethoxyphenyl)ferrocenylmethane, Fc-CH Phi(b)Phi(d) [Phi(d) = 2,4-(MeO)(2)C6H3]. The H-1-NMR spectrum of 2a was temperature-dependent and indicated that the free rotations of both Fc and Phi(a) groups in 2a existed at r.t. but were frozen at -60 degrees C. (C) 1999 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0022-328x(98)00925-5
• 作为产物：
  描述：

  高氯酸 、 ferrocenyl(2,6-dimethoxyphenyl)methanol 以 高氯酸 、 乙醚 为溶剂， 以97%的产率得到Ferrocenyl(2,6-dimethoxyphenyl)carbenium perchlorate
  参考文献：
  名称：

  Stability and reactivity of ferrocenyl(2,4,6-trimethoxyphenyl)carbenium salts

  摘要：

  Ferrocenyl(phenyl)methanols, Fc-CH Phi OH [Fc = Fe(eta(5)-C5H5)(eta(5)-C5H4), Phi(a) = 2,4,6-(MeO)(3)C6H2 (1a); Phi(b) = 2,6-(MeO)(2)C6H3 (1b)], were prepared by the reactions of Fc-CHO with Phi Li. 1a reacted with only a slight excess of perchloric acid or tetrafluoroboric acid even in methanol and in 1 M HCl acid to give dark violet crystals of the carbenium salts, [Fc-CH Phi(a)]X [X = ClO4 (2a), BF4 (2a')]. 1b reacted with these acids in diethylether to give the carbenium salts, [Fc-CH Phi(b)]X [X = ClO4 (2b), BF4 (2b') (dark red-brown crystals)] in good yields. The pK(R+) values could be measured in HCl acid for 1a (3.0) and for 1b (1.6). 2a and 2b were labile in hot 2-propanol to give the reduced compounds, Fc-CH(2)Phi. 1a and 1b reacted with 1,3,5-trimethoxybenzene, Phi(a)H, in 2-methyl-2-propanol containing only a slight excess of HCl acid to give diphenyl(ferrocenyl)methanes, Fc-CH Phi(2)(a) and Fc-CH Phi(a)Phi(b), respectively. While 1a decomposed in neat 1,3-dimethoxybenzene, Phi(b)H, in the presence of acid, 1b reacted to give 2,4-dimethoxyphenyl(2,6-dimethoxyphenyl)ferrocenylmethane, Fc-CH Phi(b)Phi(d) [Phi(d) = 2,4-(MeO)(2)C6H3]. The H-1-NMR spectrum of 2a was temperature-dependent and indicated that the free rotations of both Fc and Phi(a) groups in 2a existed at r.t. but were frozen at -60 degrees C. (C) 1999 Elsevier Science S.A. All rights reserved.

  DOI：

  10.1016/s0022-328x(98)00925-5