5-butyloxy-3-(7-methyl-2-oxo-2H-chromen-4-yl)-2H,5H-pyrano[3,2-c]chromen-2-one | 1070332-31-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: 5-butyloxy-3-(7-methyl-2-oxo-2H-chromen-4-yl)-2H,5H-pyrano[3,2-c]chromen-2-one
• 英文别名: 5-butoxy-3-(7-methyl-2-oxochromen-4-yl)-5H-pyrano[3,2-c]chromen-2-one
• CAS: 1070332-31-8
• 化学式: C₂₆H₂₂O₆
• 分子量: 430.457
• InChiKey: OQEVVXWIKUGEGV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  32
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  71.1
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  3-(7-methyl-2-oxo-2H-chromen-4-yl)-2-oxo-2H,5H-pyrano[3,2-c]chromen-5-yl acetate 、 正丁醇 在 对甲苯磺酸 作用下， 反应 2.0h， 以56%的产率得到5-butyloxy-3-(7-methyl-2-oxo-2H-chromen-4-yl)-2H,5H-pyrano[3,2-c]chromen-2-one
  参考文献：
  名称：

  Convenient synthesis and unusual reactivity of 2-oxo-2H,5H-pyrano[3,2-c]chromenes

  摘要：

  The reaction of 4-oxo-4H-chromen-3-carbaldehydes with coumarin-4-acetic acids under the Perkin conditions follows an interesting pathway that involves aldol reaction and subsequent intramolecular lactonization to afford 2-oxo-2H,5H-pyrano[3,2-c]chromene skeleton. In contrast to chromone-3-carbaldehydes, the same reaction with chromone-2-carbaldehydes yielded only the aldol condensation product. The reaction was performed under thermal and microwave conditions. The reactivity of 2-oxo2H,5H-pyrano[3,2-c]chromenes in water, alcohol and acetic acid was described. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2008.07.032

文献信息

• Convenient synthesis and unusual reactivity of 2-oxo-2H,5H-pyrano[3,2-c]chromenes
  作者：Margita Lácová、Henrieta Stankovičová、Andrej Boháč、Bibiána Kotzianová

  DOI：10.1016/j.tet.2008.07.032

  日期：2008.9

  The reaction of 4-oxo-4H-chromen-3-carbaldehydes with coumarin-4-acetic acids under the Perkin conditions follows an interesting pathway that involves aldol reaction and subsequent intramolecular lactonization to afford 2-oxo-2H,5H-pyrano[3,2-c]chromene skeleton. In contrast to chromone-3-carbaldehydes, the same reaction with chromone-2-carbaldehydes yielded only the aldol condensation product. The reaction was performed under thermal and microwave conditions. The reactivity of 2-oxo2H,5H-pyrano[3,2-c]chromenes in water, alcohol and acetic acid was described. (C) 2008 Elsevier Ltd. All rights reserved.