(1-(甲基磺酰基)哌啶-3-基)甲醇 | 349403-27-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 中文名称: (1-(甲基磺酰基)哌啶-3-基)甲醇
• 英文名称: (1-Methanesulfonylpiperidin-3-yl)methanol
• 英文别名: (1-methylsulfonylpiperidin-3-yl)methanol
• CAS: 349403-27-6
• 化学式: C₇H₁₅NO₃S
• mdl: MFCD01212952
• 分子量: 193.267
• InChiKey: UYQYZGXVWCKXLK-UHFFFAOYSA-N

物化性质

• 沸点：
  330.5±34.0 °C(Predicted)
• 密度：
  1.28±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.4
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  66
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (1-(甲基磺酰基)哌啶-3-基)甲醇 在 Celite 、 pyridinium chlorochromate 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 20.25h， 生成 3-(diphenylmethylene)-1-(methylsulfonyl)piperidine
  参考文献：
  名称：

  Synthesis of diarylazepan-4-ones

  摘要：

  Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.11.072
• 作为产物：
  描述：

  3-哌啶甲酸乙酯 在 lithium aluminium tetrahydride 、 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 9.0h， 生成 (1-(甲基磺酰基)哌啶-3-基)甲醇
  参考文献：
  名称：

  Synthesis of diarylazepan-4-ones

  摘要：

  Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.11.072

文献信息

• Synthesis of diarylazepan-4-ones
  作者：Meng-Yang Chang、Yung-Hua Kung、Chih-Chong Ma

  DOI：10.1016/j.tetlet.2006.11.072

  日期：2007.1

  Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement. (c) 2006 Elsevier Ltd. All rights reserved.