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(S)-4-hydroxy-2-methyl-N-[(R)-1-phenylethyl]butyramide | 1144099-51-3

中文名称
——
中文别名
——
英文名称
(S)-4-hydroxy-2-methyl-N-[(R)-1-phenylethyl]butyramide
英文别名
——
(S)-4-hydroxy-2-methyl-N-[(R)-1-phenylethyl]butyramide化学式
CAS
1144099-51-3
化学式
C13H19NO2
mdl
——
分子量
221.299
InChiKey
CFRKSGUHOUMJKH-WDEREUQCSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    428.5±38.0 °C(predicted)
  • 密度:
    1.057±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.88
  • 重原子数:
    16.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    49.33
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

反应信息

  • 作为产物:
    描述:
    R(+)-alpha-甲基苄胺α-甲基-γ-丁内酯甲苯 为溶剂, 反应 12.0h, 以11.4%的产率得到(R)-4-hydroxy-2-methyl-N-[(R)-1-phenylethyl]butyramide
    参考文献:
    名称:
    Seven membered ring chelates derived from γ-hydroxyamides and triphenyltin or diphenylboron
    摘要:
    N-Benzyl-4-hydroxy-butyramide (1), 4-hydroxy-N-[(R)-1-phenyl-ethyl]-butyramide (2), and (R)-4hydroxy-2-methyl-N-[(R)-1-phenyl-ethyl]-butyramide (3a) were used to prepare new diphenylboron and triphenyltinoxy compounds: diphenylborinic acid 3-benzylcarbamoyl-propyl ester (4), diphenylborinic acid 3-[(R)-1-phenyl-ethylcarbamoyl]-propyl ester (5) and diphenylborinic acid (R)-3-[(R)-1-phenyl-ethylcarbamoyl]-butyl ester (6), N-benzyl-4-triphenyltinoxy-butyramide (7), 4-triphenyltinoxy-N-[(R)-1-phenyl-ethyl]-butyramide (8), and (R)-4-triphenyltinoxy-2-methyl-N-[(R)-1-phenyl-ethyl]-butyramide (9). The X-ray diffraction analysis of a crystalline structure of the new gamma-hydroxyamide 3a is reported, as well as that of the first example of a crystalline structure where a diphenylborinic ester forms a seven membered chelate, by a carbonyl coordination to boron (4). Structural studies of tin and boron esters were performed by NMR. The C=O internal coordination to tin atoms, affording seven membered rings, was observed by Sn-119 NMR experiments at low temperature. (C) 2008 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2008.10.039
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