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3-(2-Phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole | 1023294-74-7

中文名称
——
中文别名
——
英文名称
3-(2-Phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole
英文别名
3-(2-phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole
3-(2-Phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole化学式
CAS
1023294-74-7
化学式
C22H20N2O2
mdl
——
分子量
344.413
InChiKey
HGPZAAIYBCADIM-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    43.7
  • 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:
    3-(2-Phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole铁粉氯化铵 作用下, 以 乙醇 为溶剂, 反应 6.0h, 以35%的产率得到1-(2-(benzyloxy)phenyl)-3-hydroxy-4-(pyridin-3-yl)butan-1-one
    参考文献:
    名称:
    Reduction of Δ2-Isoxazolines to β-Hydroxy Ketones with Iron and Ammonium Chloride as Reducing Agent
    摘要:
    A detailed study of a procedure for the selective reduction of Delta(2)-isoxazolines to the corresponding beta-hydroxy ketones is reported. The use of iron and ammonium chloride as the reducing agent in the presence of water results in a facile and chemoselective protocol for the preparation of beta-hydroxy ketones, including the conjugated beta-hydroxy ketones.
    DOI:
    10.1021/jo801831c
  • 作为产物:
    描述:
    3-溴吡啶 、 在 tris(dibenzylideneacetone)dipalladium (0) 、 4,5-双二苯基膦-9,9-二甲基氧杂蒽sodium t-butanolate 作用下, 以 甲苯 为溶剂, 反应 3.0h, 以89%的产率得到3-(2-Phenylmethoxyphenyl)-5-(pyridin-3-ylmethyl)-4,5-dihydro-1,2-oxazole
    参考文献:
    名称:
    Pd-Catalyzed Carboetherification of β,γ-Unsaturated Oximes: A Novel Approach to Δ2-Isoxazolines
    摘要:
    A novel route to the synthesis of Delta(2)-isoxazoline derivatives is described. Reaction of beta,gamma-unsaturated oximes with aryl bromides via palladium-catalyzed carboetherification affords 3,5-disubstituted Delta(2)-isoxazolines in good yields. The use of Xantphos as ligand is crucial for the transformation. The carboetherification products can be further converted to beta-hydroxy ketones in the presence of Fe powder and NH(4)Cl.
    DOI:
    10.1021/ol8002173
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文献信息

  • Pd-Catalyzed Carboetherification of β,γ-Unsaturated Oximes: A Novel Approach to Δ<sup>2</sup>-Isoxazolines
    作者:Dahong Jiang、Jinsong Peng、Yuanwei Chen
    DOI:10.1021/ol8002173
    日期:2008.5.1
    A novel route to the synthesis of Delta(2)-isoxazoline derivatives is described. Reaction of beta,gamma-unsaturated oximes with aryl bromides via palladium-catalyzed carboetherification affords 3,5-disubstituted Delta(2)-isoxazolines in good yields. The use of Xantphos as ligand is crucial for the transformation. The carboetherification products can be further converted to beta-hydroxy ketones in the presence of Fe powder and NH(4)Cl.
  • Reduction of Δ<sup>2</sup>-Isoxazolines to β-Hydroxy Ketones with Iron and Ammonium Chloride as Reducing Agent
    作者:Dahong Jiang、Yuanwei Chen
    DOI:10.1021/jo801831c
    日期:2008.11.21
    A detailed study of a procedure for the selective reduction of Delta(2)-isoxazolines to the corresponding beta-hydroxy ketones is reported. The use of iron and ammonium chloride as the reducing agent in the presence of water results in a facile and chemoselective protocol for the preparation of beta-hydroxy ketones, including the conjugated beta-hydroxy ketones.
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