(R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl 2-(4'''-methoxybenzyloxy)acetamide | 1234713-89-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl 2-(4'''-methoxybenzyloxy)acetamide
• CAS: 1234713-89-3
• 化学式: C₂₆H₃₁NO₄
• 分子量: 421.536
• InChiKey: SFRCBOJWGUINBG-LJQANCHMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.68
• 重原子数：
  31.0
• 可旋转键数：
  8.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  48.0
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  1-碘戊烷 、 (R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl 2-(4'''-methoxybenzyloxy)acetamide 在 18-冠醚-6 、 双(三甲基硅烷基)氨基钾 作用下， 以 四氢呋喃 为溶剂， 以87%的产率得到(R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl (S)-2-(4'''-methoxybenzyloxy)heptanamide
  参考文献：
  名称：

  Alkylation and aldol reactions of acyl derivatives of N-1-(1′-naphthyl)ethyl-O-tert-butylhydroxylamine: asymmetric synthesis of α-alkoxy-, α-substituted-β-alkoxy- and α,β-dialkoxyaldehydes

  摘要：

  Treatment of a range of O-protected glycolate derivatives of the chiral auxiliary N-1-(1'-naphthyl)ethyl-O-tert-butylhydroxylamine with KHMDS in the presence of 18-crown-6 followed by addition of an alkyl halide generates alpha-substituted derivatives with very high levels of diastereoselectivity. Alternatively, reaction of the potassium enolate of a propanoate or O-protected glycolate derivative of N-1-(1'-naphthyl)ethyl-O-tert-butylhydroxylamine with a range of aldehydes gives syn-aldol products with high levels of diastereoselectivity. These adducts may be reductively cleaved with LiAlH(4) to give enantiopure alpha-alkoxy-, alpha-substituted-beta-alkoxy- and alpha,beta-dialkoxyaldehydes in good yield. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.03.105
• 作为产物：
  描述：

  (R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl 2-bromoacetamide 、 4-甲氧基苄醇 在 sodium hydride 、 15-冠醚-5 、 四丁基碘化铵 作用下， 以 四氢呋喃 为溶剂， 反应 3.17h， 以61%的产率得到(R)-N-tert-butoxy-N-1'-(1''-naphthyl)ethyl 2-(4'''-methoxybenzyloxy)acetamide
  参考文献：
  名称：

  Alkylation and aldol reactions of acyl derivatives of N-1-(1′-naphthyl)ethyl-O-tert-butylhydroxylamine: asymmetric synthesis of α-alkoxy-, α-substituted-β-alkoxy- and α,β-dialkoxyaldehydes

  摘要：

  Treatment of a range of O-protected glycolate derivatives of the chiral auxiliary N-1-(1'-naphthyl)ethyl-O-tert-butylhydroxylamine with KHMDS in the presence of 18-crown-6 followed by addition of an alkyl halide generates alpha-substituted derivatives with very high levels of diastereoselectivity. Alternatively, reaction of the potassium enolate of a propanoate or O-protected glycolate derivative of N-1-(1'-naphthyl)ethyl-O-tert-butylhydroxylamine with a range of aldehydes gives syn-aldol products with high levels of diastereoselectivity. These adducts may be reductively cleaved with LiAlH(4) to give enantiopure alpha-alkoxy-, alpha-substituted-beta-alkoxy- and alpha,beta-dialkoxyaldehydes in good yield. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.03.105