(S)-benzyl (1-hydroxyhexan-2-yl)(methyl)carbamate | 1445443-38-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (S)-benzyl (1-hydroxyhexan-2-yl)(methyl)carbamate
• 英文别名: benzyl N-[(2S)-1-hydroxyhexan-2-yl]-N-methylcarbamate
• CAS: 1445443-38-8
• 化学式: C₁₅H₂₃NO₃
• 分子量: 265.353
• InChiKey: HNZWQXYPFQYHOU-AWEZNQCLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  19
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  49.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-benzyl (1-hydroxyhexan-2-yl)(methyl)carbamate 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 0.67h， 生成 benzyl N-methyl-N-[(2S)-1-oxohexan-2-yl]carbamate
  参考文献：
  名称：

  A Mild Multistep Conversion of N-Protected α-Amino Acids into N-Protected β3-Amino Acids Utilizing the Nef Reaction

  摘要：

  Current methods of homologation of alpha-amino acids to beta-amino acids have limitations. To overcome these shortfalls the Nef reaction has been utilized in the multistep synthesis of beta(3)-amino acids from alpha-amino acids. In this approach, N-protected amino aldehydes, easily accessed from alpha-amino acids, were transformed into the N-protected.gamma-amino nitroalkanes. The Nef reaction was then used to smoothly convert the nitroalkanes into the corresponding N-protected beta(3)-amino acids without notable racemization.

  DOI：

  10.1055/s-0032-1318344
• 作为产物：
  描述：

  Z-n-me-l-2-氨基己酸 在 N-甲基吗啉 、 sodium tetrahydroborate 作用下， 以 四氢呋喃 、 甲醇 、 水 为溶剂， 反应 0.5h， 生成 (S)-benzyl (1-hydroxyhexan-2-yl)(methyl)carbamate
  参考文献：
  名称：

  A Mild Multistep Conversion of N-Protected α-Amino Acids into N-Protected β3-Amino Acids Utilizing the Nef Reaction

  摘要：

  Current methods of homologation of alpha-amino acids to beta-amino acids have limitations. To overcome these shortfalls the Nef reaction has been utilized in the multistep synthesis of beta(3)-amino acids from alpha-amino acids. In this approach, N-protected amino aldehydes, easily accessed from alpha-amino acids, were transformed into the N-protected.gamma-amino nitroalkanes. The Nef reaction was then used to smoothly convert the nitroalkanes into the corresponding N-protected beta(3)-amino acids without notable racemization.

  DOI：

  10.1055/s-0032-1318344

文献信息

• A Mild Multistep Conversion of N-Protected α-Amino Acids into N-Protected β3-Amino Acids Utilizing the Nef Reaction
  作者：Andrew Hughes、Brad Sleebs、Nghi Nguyen

  DOI：10.1055/s-0032-1318344

  日期：——

  Current methods of homologation of alpha-amino acids to beta-amino acids have limitations. To overcome these shortfalls the Nef reaction has been utilized in the multistep synthesis of beta(3)-amino acids from alpha-amino acids. In this approach, N-protected amino aldehydes, easily accessed from alpha-amino acids, were transformed into the N-protected.gamma-amino nitroalkanes. The Nef reaction was then used to smoothly convert the nitroalkanes into the corresponding N-protected beta(3)-amino acids without notable racemization.