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Methyl 2-(2-phenylethyl)-4-oxazolecarboxylate | 80314-39-2

中文名称
——
中文别名
——
英文名称
Methyl 2-(2-phenylethyl)-4-oxazolecarboxylate
英文别名
4-carbomethoxy-2-(2-phenethyl)oxazole;Methyl 2-(2-phenylethyl)-1,3-oxazole-4-carboxylate
Methyl 2-(2-phenylethyl)-4-oxazolecarboxylate化学式
CAS
80314-39-2
化学式
C13H13NO3
mdl
——
分子量
231.251
InChiKey
AQNFIZDNSAHEQL-UHFFFAOYSA-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:
    347.4±25.0 °C(Predicted)
  • 密度:
    1.174±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    52.3
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    Methyl 2-(2-phenylethyl)-4-oxazolecarboxylatesilver(I) acetate 、 palladium diacetate 作用下, 以 二甲基亚砜N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 以69%的产率得到dimethyl 2,2'-diphenylethyl-bis-5,5'-oxazole-4,4'-dicarboxylate
    参考文献:
    名称:
    Efficient palladium(II)-catalyzed homocoupling of thiazole-4-carboxylic or oxazole-4-carboxylic derivatives
    摘要:
    An efficient Pd(OAc)(2)-catalyzed homocoupling of thiazole-4-carboxylic or oxazole-4-carboxylic derivatives is described. It represents a facile and practical methodology to prepare bis-5,5'-thiazole (oxazole)-4,4'-dicarboxylic derivatives in good to excellent yields. This protocol tolerates a series of substitutions on the thiazole (oxazole) rings, including alkyl, carbonyl, and electron-withdrawing/donating group substituted phenyl groups. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.123
  • 作为产物:
    参考文献:
    名称:
    Dimethyl amino[(phenylthio)methyl]malonate: a useful C-3 unit in a mild, direct synthesis of oxazole-4-carboxylates
    摘要:
    N-Acyl derivatives of the title compound undergo oxidative cyclization upon treatment with N-chlorosuccinimide in DMF to form dimethyl 4,5-dihydro(phenylthio)oxazole-4,4-dicarboxylates 4 which then are decarbomethoxylated with concomitant loss of thiophenoxide to form 2-substituted-4-carbomethoxy-5-unsubstituted oxazoles 1. The mildness and generality of this method has been demonstrated by the synthesis of a variety of examples, including a fragment used for a synthesis of calyculin A.
    DOI:
    10.1021/jo00073a040
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文献信息

  • Synthetic studies on the streptogramin antibiotics. Enantioselective synthesis of the oxazole dienyl amine moiety
    作者:A. I. Meyers、J. P. Lawson、D. G. Walker、R. J. Linderman
    DOI:10.1021/jo00376a011
    日期:1986.12
  • Anomalous metalation behavior in 1,3-oxazoles. Alkylation of 2-methyl-4-carboxyoxazoles via the cornforth intermediate
    作者:A.I. Meyers、Jon P. Lawson
    DOI:10.1016/s0040-4039(01)81853-0
    日期:1981.1
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