1-(4-hydroxy-3-methoxyphenyl)-4-methyl-3-pentanone | 452528-73-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 1-(4-hydroxy-3-methoxyphenyl)-4-methyl-3-pentanone
• 英文别名: 1-(4-Hydroxy-3-methoxyphenyl)-4-methylpentan-3-one；1-(4-hydroxy-3-methoxyphenyl)-4-methylpentan-3-one
• CAS: 452528-73-3
• 化学式: C₁₃H₁₈O₃
• 分子量: 222.284
• InChiKey: UUAPKYXCTFBKFF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(4-hydroxy-3-methoxyphenyl)-4-methyl-3-pentanone 在 lead(IV) acetate 、 sodium tetrahydroborate 作用下， 以 乙醇 、 丙酮 为溶剂， 反应 2.5h， 生成 2-Isopropyl-7-methoxy-1-oxa-spiro[4.5]deca-6,9-dien-8-one
  参考文献：
  名称：

  Studies towards the diastereoselective spiroannulation of phenolic derivatives

  摘要：

  The oxidative spiroannulation of simple phenols bearing a chiral center was carried out. Good yields (61-83%) of spirocompounds were obtained. An increase in diastereomeric ratios front 55/45 to 81/19 was observed as the steric factor Surrounding the chiral carbon increased. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(02)00552-x
• 作为产物：
  描述：

  4-苄氧基-3-甲氧基苯甲醛 在 palladium on activated charcoal 氢气 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 乙酸乙酯 为溶剂， 生成 1-(4-hydroxy-3-methoxyphenyl)-4-methyl-3-pentanone
  参考文献：
  名称：

  Studies towards the diastereoselective spiroannulation of phenolic derivatives

  摘要：

  The oxidative spiroannulation of simple phenols bearing a chiral center was carried out. Good yields (61-83%) of spirocompounds were obtained. An increase in diastereomeric ratios front 55/45 to 81/19 was observed as the steric factor Surrounding the chiral carbon increased. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(02)00552-x

文献信息

• Studies towards the diastereoselective spiroannulation of phenolic derivatives
  作者：Guy L. Plourde

  DOI：10.1016/s0040-4039(02)00552-x

  日期：2002.5

  The oxidative spiroannulation of simple phenols bearing a chiral center was carried out. Good yields (61-83%) of spirocompounds were obtained. An increase in diastereomeric ratios front 55/45 to 81/19 was observed as the steric factor Surrounding the chiral carbon increased. (C) 2002 Elsevier Science Ltd. All rights reserved.