diethyl {3-[3-hydroxy-2-(hydroxymethyl)propyl]phenyl}methylphosphonate | 213127-74-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物
• 英文名称: diethyl {3-[3-hydroxy-2-(hydroxymethyl)propyl]phenyl}methylphosphonate
• 英文别名: 2-[[3-(Diethoxyphosphorylmethyl)phenyl]methyl]propane-1,3-diol
• CAS: 213127-74-3
• 化学式: C₁₅H₂₅O₅P
• 分子量: 316.334
• InChiKey: CWAMVEYUFMKUGV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  21
• 可旋转键数：
  10
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  76
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  diethyl {3-[3-hydroxy-2-(hydroxymethyl)propyl]phenyl}methylphosphonate 在 Lipase PS 、 三(2-氯乙基)胺 、 偶氮二甲酸二异丙酯 、 三苯基膦 作用下， 以 四氢呋喃 、 硫酸 、 苯 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  Enzymatic desymmetrization of prochiral 2-benzyl-1,3-propanediol derivatives: A practical chemoenzymatic synthesis of novel phosphorylated tyrosine analogues

  摘要：

  (Phosphonomethyl)phenylalanine (Pmp) and (phosphonodifluoromethyl)phenylalanine (F(2)Pmp) as well as their beta-amino acid congeners were prepared as a protecting variant amenable to the peptide synthesis from readily available 2-benzyl-1,3-propandiols possessing either a diethylphosphonomethyl- or diethylphosphonodifluoromethyl functionality at the para-position via the lipase-catalyzed desymmetrization. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00586-9
• 作为产物：
  描述：

  dimethyl 2-[3-(diethoxyphosphorylmethyl)benzyl]malonate 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以90%的产率得到diethyl {3-[3-hydroxy-2-(hydroxymethyl)propyl]phenyl}methylphosphonate
  参考文献：
  名称：

  Enzymatic desymmetrization of prochiral 2-benzyl-1,3-propanediol derivatives: A practical chemoenzymatic synthesis of novel phosphorylated tyrosine analogues

  摘要：

  (Phosphonomethyl)phenylalanine (Pmp) and (phosphonodifluoromethyl)phenylalanine (F(2)Pmp) as well as their beta-amino acid congeners were prepared as a protecting variant amenable to the peptide synthesis from readily available 2-benzyl-1,3-propandiols possessing either a diethylphosphonomethyl- or diethylphosphonodifluoromethyl functionality at the para-position via the lipase-catalyzed desymmetrization. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(98)00586-9