4-tert-butyl-6-nitrosoresorcinol | 167315-94-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-tert-butyl-6-nitrosoresorcinol
• 英文别名: 4-Tert-butyl-6-nitrosobenzene-1,3-diol
• CAS: 167315-94-8
• 化学式: C₁₀H₁₃NO₃
• 分子量: 195.218
• InChiKey: JNOGPCIXYPHUAT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  69.9
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-tert-butyl-6-nitrosoresorcinol 在 tin(ll) chloride 作用下， 以 乙醇 、 乙腈 为溶剂， 反应 5.5h， 生成 4-tert-Butyl-6-{[1-phenyl-meth-(E)-ylidene]-amino}-benzene-1,3-diol
  参考文献：
  名称：

  Model Studies of Topaquinone-Dependent Amine Oxidases. 2. Characterization of Reaction Intermediates and Mechanism

  摘要：

  The reaction of 2-hydroxy-5-tert-butyl-1,4-benzoquinone (1a) and benzylamine in acetonitrile was studied under anaerobic conditions. Addition of benzylamine to the quinone 1a solution generates the anionic form of the quinone (lambda(max) at 492 nm), followed by the formation of the product Schiff base 11 with lambda(max) at 368 nm and the aminoresorcinol 13 with lambda(max) at 304 nm. The rapid dissociation of the 2-hydroxyl proton was confirmed by the isolation of the amine salt 5a in the reaction of tert-butylamine and 1a. The substrate Schiff base 6a was not spectrally detected due to its lower extinction coefficient and rapid conversion to the product Schiff base 11. However, when alpha-methylbenzylamine was employed as a substrate, the formation of the substrate Schiff base 7 was detected by H-1 NMR and W-vis spectroscopy, Cyclohexylamine, n-propylamine, and ammonia also gave the substrate Schiff bases 8, 9, and 10, respectively, Both the steric bulk and the acidity of the C-1 proton of the substrate are found to be factors controlling the further reaction (C-1 proton abstraction). Detailed structural analysis of the substrate Schiff base was performed on 8 by 2D NMR spectroscopy, showing that 8 is in its amine salt form and has undergone nucleophilic addition at C-1, the carbonyl carbon next to the 2-hydroxyl group. W-vis spectroscopy supports the view that 8 is not a solvent-separated ion pair (lambda(max) at 454 nm) but an intimate ion pair (lambda(max) at 352 nm) in CH3CN. The latter lambda(max) value is very similar to lambda(max) observed for the Schiff base complex seen in bovine serum amine oxidase and different from a Schiff base complex with 4-methoxy-5-tert-butyl-1,2-benzoquinone 14. The product Schiff base 11 was prepared by the reaction of the hydrochloride salt of the aminoresorcinol 13 and benzaldehyde. It has an epsilon value 10 times larger than that of the substrate Schiff base (7, 8, or 9) at 368 nm. Treatment of 11 with benzylamine yielded the aminoresorcinol 13 and the product, N-benzylidenebenzylamine (PhCH=NCH(2)Ph). Comparison of these results to catalytic properties of the copper amine oxidases provides support for an aminotransferase mechanism from a Schiff base of topa in a localized p-quinone form (B in Scheme 1).

  DOI：

  10.1021/ja00139a003
• 作为产物：
  描述：

  4-叔-丁基苯-1,3-二醇 在 盐酸 、 sodium nitrite 作用下， 以 乙醇 为溶剂， 反应 0.25h， 以70%的产率得到4-tert-butyl-6-nitrosoresorcinol
  参考文献：
  名称：

  Model Studies of Topaquinone-Dependent Amine Oxidases. 2. Characterization of Reaction Intermediates and Mechanism

  摘要：

  The reaction of 2-hydroxy-5-tert-butyl-1,4-benzoquinone (1a) and benzylamine in acetonitrile was studied under anaerobic conditions. Addition of benzylamine to the quinone 1a solution generates the anionic form of the quinone (lambda(max) at 492 nm), followed by the formation of the product Schiff base 11 with lambda(max) at 368 nm and the aminoresorcinol 13 with lambda(max) at 304 nm. The rapid dissociation of the 2-hydroxyl proton was confirmed by the isolation of the amine salt 5a in the reaction of tert-butylamine and 1a. The substrate Schiff base 6a was not spectrally detected due to its lower extinction coefficient and rapid conversion to the product Schiff base 11. However, when alpha-methylbenzylamine was employed as a substrate, the formation of the substrate Schiff base 7 was detected by H-1 NMR and W-vis spectroscopy, Cyclohexylamine, n-propylamine, and ammonia also gave the substrate Schiff bases 8, 9, and 10, respectively, Both the steric bulk and the acidity of the C-1 proton of the substrate are found to be factors controlling the further reaction (C-1 proton abstraction). Detailed structural analysis of the substrate Schiff base was performed on 8 by 2D NMR spectroscopy, showing that 8 is in its amine salt form and has undergone nucleophilic addition at C-1, the carbonyl carbon next to the 2-hydroxyl group. W-vis spectroscopy supports the view that 8 is not a solvent-separated ion pair (lambda(max) at 454 nm) but an intimate ion pair (lambda(max) at 352 nm) in CH3CN. The latter lambda(max) value is very similar to lambda(max) observed for the Schiff base complex seen in bovine serum amine oxidase and different from a Schiff base complex with 4-methoxy-5-tert-butyl-1,2-benzoquinone 14. The product Schiff base 11 was prepared by the reaction of the hydrochloride salt of the aminoresorcinol 13 and benzaldehyde. It has an epsilon value 10 times larger than that of the substrate Schiff base (7, 8, or 9) at 368 nm. Treatment of 11 with benzylamine yielded the aminoresorcinol 13 and the product, N-benzylidenebenzylamine (PhCH=NCH(2)Ph). Comparison of these results to catalytic properties of the copper amine oxidases provides support for an aminotransferase mechanism from a Schiff base of topa in a localized p-quinone form (B in Scheme 1).

  DOI：

  10.1021/ja00139a003