3-(3,4-dimethyl-phenoxy)-propane-1,2-diol | 5469-71-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 3-(3,4-dimethyl-phenoxy)-propane-1,2-diol
• 英文别名: 3-(3,4-Dimethyl-phenoxy)-propan-1,2-diol；3-(3,4-Dimethylphenoxy)propane-1,2-diol
• CAS: 5469-71-6
• 化学式: C₁₁H₁₆O₃
• 分子量: 196.246
• InChiKey: RRPWOUKAVFCTKN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  49.7
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 海关编码：
  2909499000

反应信息

• 作为反应物：
  描述：

  3-(3,4-dimethyl-phenoxy)-propane-1,2-diol 在 吡啶 、 盐酸 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 乙醇 、 丙酮 为溶剂， 反应 28.0h， 生成 1-(3,4-dimethylphenoxy)-3-(morpholin-4-yl)propan-2-ol hydrochloride
  参考文献：
  名称：

  Nonracemic Dimethylphenyl Glycerol Ethers in the Synthesis of Physiologically Active Aminopropanols

  摘要：

  Six regioisomeric nonracemic dimethylphenyl glycerol ethers were synthesized by asymmetric dihydroxylation of the corresponding allyl dimethylphenyl ethers. The enantioselectivity of the reaction with o-methyl derivatives was lower (down to 34% ee) than with m-methylphenyl ethers (up to 86% ee). Enantiomeric 3-(3,4-dimethylphenoxy)propane-1,2-diols were used to obtain enantiomerically pure physiologically active amino alcohols and their derivatives.

  DOI：

  10.1134/s1070428019060149
• 作为产物：
  描述：

  3,4-二甲基苯酚 、 3-氯-1,2-丙二醇 在 sodium hydroxide 作用下， 生成 3-(3,4-dimethyl-phenoxy)-propane-1,2-diol
  参考文献：
  名称：

  Muscle-Relaxing Compounds Similar to 3-(o-Toloxy)-1,2-propanediol. II. Substituted Alkanediols¹

  摘要：

  DOI：

  10.1021/ja01164a108

文献信息

• 5-Aryloxymethyl-2-oxazolidinones
  作者：Carl D. Lunsford、Richard P. Mays、John A. Richman、Robert S. Murphey

  DOI：10.1021/ja01490a037

  日期：1960.3
• Muscle-Relaxing Compounds Similar to 3-(o-Toloxy)-1,2-propanediol. II. Substituted Alkanediols¹
  作者：Harry L. Yale、Edward J. Pribyl、William Braker、Jack Bernstein、W. A. Lott

  DOI：10.1021/ja01164a108

  日期：1950.8
• Nonracemic Dimethylphenyl Glycerol Ethers in the Synthesis of Physiologically Active Aminopropanols
  作者：Z. A. Bredikhina、A. V. Kurenkov、A. A. Bredikhin

  DOI：10.1134/s1070428019060149

  日期：2019.6

  Six regioisomeric nonracemic dimethylphenyl glycerol ethers were synthesized by asymmetric dihydroxylation of the corresponding allyl dimethylphenyl ethers. The enantioselectivity of the reaction with o-methyl derivatives was lower (down to 34% ee) than with m-methylphenyl ethers (up to 86% ee). Enantiomeric 3-(3,4-dimethylphenoxy)propane-1,2-diols were used to obtain enantiomerically pure physiologically active amino alcohols and their derivatives.