1-Diethoxyphosphoryl-3-methylbutan-2-ol | 20030-52-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机膦酸及其衍生物
• 英文名称: 1-Diethoxyphosphoryl-3-methylbutan-2-ol
• CAS: 20030-52-8
• 化学式: C₉H₂₁O₄P
• 分子量: 224.237
• InChiKey: DBMJCINPPMRMNO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  14
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  55.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-Diethoxyphosphoryl-3-methylbutan-2-ol 在 N,N'-二环己基碳二亚胺 、 copper dichloride 作用下， 以 甲苯 为溶剂， 反应 6.0h， 以65%的产率得到(E)-(3-methylbut-1-enyl)phosphonic acid diethyl ester
  参考文献：
  名称：

  A Convenient (E)-Stereoselective Synthesis of Alkenylphosphonates

  摘要：

  Diethyl (E)-alkenylphosphonates have been prepared stereoselectively by dehydration of the corresponding beta-hydroxyphosphonates using DCC/CuCl2 in refluxing toluene. Starting beta-hydroxyphosphonates were obtained in high yield from diethyl methylphosphonate.

  DOI：

  10.1080/00397919708005031
• 作为产物：
  描述：

  甲基膦酸二乙酯 在 正丁基锂 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 0.17h， 生成 1-Diethoxyphosphoryl-3-methylbutan-2-ol
  参考文献：
  名称：

  A Convenient (E)-Stereoselective Synthesis of Alkenylphosphonates

  摘要：

  Diethyl (E)-alkenylphosphonates have been prepared stereoselectively by dehydration of the corresponding beta-hydroxyphosphonates using DCC/CuCl2 in refluxing toluene. Starting beta-hydroxyphosphonates were obtained in high yield from diethyl methylphosphonate.

  DOI：

  10.1080/00397919708005031

文献信息

• A new entry to β-hydroxyphosphonates: the SmI2-mediated reaction of diethyl iodomethylphosphonate with carbonyl compounds
  作者：Fulvia Orsini、Alessandro Caselli

  DOI：10.1016/s0040-4039(02)01539-3

  日期：2002.9

  In the presence of samarium iodide α-halophosphonates react with aliphatic carbonyl compounds (aldehydes and ketones) to afford β-hydroxyphosphonates in fairly good yields under neutral and mild conditions. Lower yields are obtained with aromatic carbonyl compounds.

  在碘化sa的存在下，α-卤代膦酸酯与脂肪族羰基化合物（醛和酮）反应，在中性和温和条件下以相当好的收率得到β-羟基膦酸酯。用芳族羰基化合物获得较低的收率。
• Dynamic kinetic resolution of α-chloro β-keto esters and phosphonates: hemisynthesis of Taxotere® through Ru-DIFLUORPHOS asymmetric hydrogenation
  作者：Sébastien Prévost、Sébastien Gauthier、Maria Cristina Caño de Andrade、Céline Mordant、Ali Rhida Touati、Philippe Lesot、Philippe Savignac、Tahar Ayad、Phannarath Phansavath、Virginie Ratovelomanana-Vidal、Jean-Pierre Genêt

  DOI：10.1016/j.tetasy.2010.05.017

  日期：2010.6

  The dynamic kinetic resolution (DKR) of racemic alpha-chloro beta-ketoesters and alpha-chloro beta-ketophosphonates through ruthenium-mediated asymmetric hydrogenation is reported. The corresponding alpha-chloro beta-hydroxyesters and alpha-chloro beta-hydroxyphosphonates were obtained in good to high enantio- and diastereomeric excesses using, in particular, the atropisomeric ligand DIFLUORPHOS. This methodology allowed an efficient preparation of the anti phenylisoserine side chain of Taxotere (R) which has been used for the hemisynthesis of the cancer therapeutic agent itself. In addition, C-13 NMR in chiral oriented solvents was used to investigate the DKR effect. (C) 2010 Elsevier Ltd. All rights reserved.
• Reformatsky reactions with SmI2 in catalytic amount
  作者：Fulvia Orsini、Elvira Maria Lucci

  DOI：10.1016/j.tetlet.2005.01.079

  日期：2005.3

  A substoichiometric protocol for Reformatsky-type addition of alpha-haloesters, alpha-haloketones, alpha-halonitriles, and alpha-halophosphonates to carbonyl compounds has been developed. beta-Hydroxyesters and beta-hydroxynitriles were obtained in good to excellent yields. (C) 2005 Elsevier Ltd. All rights reserved.
• A Convenient (E)-Stereoselective Synthesis of Alkenylphosphonates
  作者：Isabelle Truel、Abdourahman Mohamed-Hachi、Elie About-Jaudet、Noël Collignon

  DOI：10.1080/00397919708005031

  日期：1997.1

  Diethyl (E)-alkenylphosphonates have been prepared stereoselectively by dehydration of the corresponding beta-hydroxyphosphonates using DCC/CuCl2 in refluxing toluene. Starting beta-hydroxyphosphonates were obtained in high yield from diethyl methylphosphonate.