3-(2-Hydroxy-ethyl)-5-methoxymethoxy-7-pentyl-chromen-2-one | 137060-00-5

• 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: 3-(2-Hydroxy-ethyl)-5-methoxymethoxy-7-pentyl-chromen-2-one
• 英文别名: 3-(2-hydroxyethyl)-5-(methoxymethoxy)-7-pentylchromen-2-one
• CAS: 137060-00-5
• 化学式: C₁₈H₂₄O₅
• 分子量: 320.386
• InChiKey: YWWLDHBQPGPEDG-UHFFFAOYSA-N

物化性质

• 沸点：
  499.2±45.0 °C(Predicted)
• 密度：
  1.146±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.04
• 重原子数：
  23.0
• 可旋转键数：
  9.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  68.9
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  3-(2-Hydroxy-ethyl)-5-methoxymethoxy-7-pentyl-chromen-2-one 在 triphenylphosphine dibromide 1:1 addition complex 作用下， 以 乙腈 为溶剂， 反应 3.0h， 以73%的产率得到3-(2-Bromo-ethyl)-5-hydroxy-7-pentyl-chromen-2-one
  参考文献：
  名称：

  3-Vinylcoumarins and 3-vinylchromenes as dienes. Application to the synthesis of 3,4-fused coumarins and chromenes

  摘要：

  The reaction of alpha-(diethylphosphono)-gamma-butyrolactones 1 with o-hydroxyaryl aldehydes 2 and 7 gave 3-(2-hydroxyethyl)coumarins 3 in excellent yields. Treatment of 3 or 3-(2-hydroxyethyl)-2,2-dimethylchromenes 11 derived from 3 with triphenylphosphine dibromide led to the corresponding 3-(2-bromoethyl)coumarins 8 or 3-(2-bromoethyl)chromenes 12 in good yields. The Diels-Alder reaction of the 3-vinylcoumarins 13 or the 3-vinylchromenes 31, generated in situ from treatment of the bromides 8 or 12 with DBU, with a variety of dienophiles 14-19 and 35 produced regiospecific [2 + 4] cycloadducts, 3,4-fused coumarins 20-28 or 3,4-fused chromenes 32-34 and 36 in good to moderate yields.

  DOI：

  10.1021/jo00027a032
• 作为产物：
  描述：

  2-formyl-5-pentylresorcinol 1,3-bis-(methoxymethyl) ether 在 盐酸 、 sodium hydride 作用下， 以 四氢呋喃 为溶剂， 反应 7.0h， 生成 3-(2-Hydroxy-ethyl)-5-methoxymethoxy-7-pentyl-chromen-2-one
  参考文献：
  名称：

  3-Vinylcoumarins and 3-vinylchromenes as dienes. Application to the synthesis of 3,4-fused coumarins and chromenes

  摘要：

  The reaction of alpha-(diethylphosphono)-gamma-butyrolactones 1 with o-hydroxyaryl aldehydes 2 and 7 gave 3-(2-hydroxyethyl)coumarins 3 in excellent yields. Treatment of 3 or 3-(2-hydroxyethyl)-2,2-dimethylchromenes 11 derived from 3 with triphenylphosphine dibromide led to the corresponding 3-(2-bromoethyl)coumarins 8 or 3-(2-bromoethyl)chromenes 12 in good yields. The Diels-Alder reaction of the 3-vinylcoumarins 13 or the 3-vinylchromenes 31, generated in situ from treatment of the bromides 8 or 12 with DBU, with a variety of dienophiles 14-19 and 35 produced regiospecific [2 + 4] cycloadducts, 3,4-fused coumarins 20-28 or 3,4-fused chromenes 32-34 and 36 in good to moderate yields.

  DOI：

  10.1021/jo00027a032