2,4,6-triethylisophthalaldehyde | 135779-06-5

• 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: 2,4,6-triethylisophthalaldehyde
• 英文别名: 1,3-diformyl-2,4,6-triethylbenzene；2,4,6-triethylbenzene-1,3-dicarbaldehyde
• CAS: 135779-06-5
• 化学式: C₁₄H₁₈O₂
• 分子量: 218.296
• InChiKey: BUPRHSJHRDYCHJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2,4,6-triethylisophthalaldehyde 在 sodium hydroxide 、 sodium hypochlorite 、 盐酸羟胺 作用下， 以 乙醇 、 二氯甲烷 、 水 为溶剂， 反应 5.0h， 生成 1,3-dicyano-2,4,6-triethyl-benzene N,N'-dioxide
  参考文献：
  名称：

  Synthesis of stable functionally substituted nitrile oxides of the aromatic series

  摘要：

  Stable functionally substituted mononitrile oxides were obtained from the previously obtained sterically hindered aldehydes of the mesitylene series. The previously unknown bisnitrile oxide was also synthesized from triethylbenzene; the compound is an effective crosslinking agent. The synthesis was carried out via the stage of oximation and oxidation of the oxime by sodium hypochlorite.

  DOI：

  10.1007/bf00961380
• 作为产物：
  描述：

  2,4,6-triethylbenzaldehyde 在 盐酸 、 五氯化磷 、 四氯化钛 、 正丁醇 作用下， 以 二氯甲烷 为溶剂， 反应 25.0h， 生成 2,4,6-triethylisophthalaldehyde
  参考文献：
  名称：

  Synthesis of sterically hindered aromatic aldehydes

  摘要：

  Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4. A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.

  DOI：

  10.1007/bf00961246

文献信息

• YAKUBOV, A. P.;TSYGANOV, D. V.;BELENKIJ, L. I.;KRAYUSHKIN, M. M., IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1201-1203
  作者：YAKUBOV, A. P.、TSYGANOV, D. V.、BELENKIJ, L. I.、KRAYUSHKIN, M. M.

  DOI：——

  日期：——
• YAKUBOV, A. P.;TSYGANOV, D. V.;BELENKIJ, L. I.;KRAYUSHKIN, M. M., IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1609-1615
  作者：YAKUBOV, A. P.、TSYGANOV, D. V.、BELENKIJ, L. I.、KRAYUSHKIN, M. M.

  DOI：——

  日期：——
• Optimization of Oxidative Method for Synthesis of 1,3-Diformyl-2,4,6-triethylbenzene
  作者：S. B. Apel'chugin、I. B. Krauklish、A. E. Punin、G. I. Tsypin

  DOI：10.1023/b:rjac.0000008300.47315.75

  日期：2003.8

  Oxidation of 1,3-diformyl-2,4,6-triethylbenzene with chromium anhydride in diluted H2SO4 to form 1,3-di(hydroxymethyl)-2,4,6-triethylbenzene was studied.
• Synthesis of sterically hindered aromatic aldehydes
  作者：A. P. Yakubov、D. V. Tsyganov、L. I. Belen'kii、M. M. Krayushkin

  DOI：10.1007/bf00961246

  日期：1991.7

  Formylation of mesitylene, durene, and m-xylene derivatives containing electron-donor and electron-acceptor substituents by dichloromethyl methyl ether was studied in the presence of TiCl4. A series of functionally substituted sterically hindered benzaldehydes was prepared from the products of these reactions.
• Synthesis of stable functionally substituted nitrile oxides of the aromatic series
  作者：A. P. Yakubov、D. V. Tsyganov、L. I. Belen'kii、M. M. Krayushkin

  DOI：10.1007/bf00961380

  日期：1991.5

  Stable functionally substituted mononitrile oxides were obtained from the previously obtained sterically hindered aldehydes of the mesitylene series. The previously unknown bisnitrile oxide was also synthesized from triethylbenzene; the compound is an effective crosslinking agent. The synthesis was carried out via the stage of oximation and oxidation of the oxime by sodium hypochlorite.