dimethyl (6-bromo-2-oxohexyl)phosphonate

• 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: dimethyl (6-bromo-2-oxohexyl)phosphonate
• 英文别名: 6-Bromo-1-[dimethoxy(oxido)phosphaniumyl]hexan-2-one；6-bromo-1-[dimethoxy(oxido)phosphaniumyl]hexan-2-one
• 化学式: C₈H₁₆BrO₄P
• 分子量: 287.09
• InChiKey: GZAPUJLJSSTNEU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  14
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.88
• 拓扑面积：
  58.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  5-溴戊酸 在 4-二甲氨基吡啶 、 正丁基锂 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 四氢呋喃 、 正己烷 、 二氯甲烷 为溶剂， 反应 2.0h， 生成 dimethyl (6-bromo-2-oxohexyl)phosphonate
  参考文献：
  名称：

  Chemoselective Synthesis of β-Ketophosphonates Using Lithiated α-(Trimethylsilyl)methylphosphonate

  摘要：

  A highly chemoselective synthesis of beta-ketophosphonates from pentafluorophenyl esters and lithiated methyl alpha-(trimethylsilyl)methylphosphonate has been developed. This mild lithiated phosphonate reagent allows the synthesis of functionalized beta-ketophosphonates in the presence of unactivated esters with high yields. This method has been compared with the standard lithiated methylphosphonate reagent.

  DOI：

  10.1021/acs.joc.5b00039

文献信息

• Chemoselective Synthesis of β-Ketophosphonates Using Lithiated α-(Trimethylsilyl)methylphosphonate
  作者：Simon Specklin、Janine Cossy

  DOI：10.1021/acs.joc.5b00039

  日期：2015.3.20

  A highly chemoselective synthesis of beta-ketophosphonates from pentafluorophenyl esters and lithiated methyl alpha-(trimethylsilyl)methylphosphonate has been developed. This mild lithiated phosphonate reagent allows the synthesis of functionalized beta-ketophosphonates in the presence of unactivated esters with high yields. This method has been compared with the standard lithiated methylphosphonate reagent.