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2-(2,3-dihydroxy)propyl-4-propoxymethylbutanolide | 945738-27-2

中文名称
——
中文别名
——
英文名称
2-(2,3-dihydroxy)propyl-4-propoxymethylbutanolide
英文别名
——
2-(2,3-dihydroxy)propyl-4-propoxymethylbutanolide化学式
CAS
945738-27-2
化学式
C11H20O5
mdl
——
分子量
232.277
InChiKey
JWUREBVWOZDLAM-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

反应信息

  • 作为反应物:
    描述:
    2-(2,3-dihydroxy)propyl-4-propoxymethylbutanolideN-溴代丁二酰亚胺(NBS) 作用下, 以 丙酮 为溶剂, 反应 5.0h, 以70%的产率得到2-(3-bromo-2-hydroxypropyl)-4-propoxymethylbutanolide
    参考文献:
    名称:
    Synthesis and some transformations of 2-alkenyl-4-alkoxymethylbutanolides
    摘要:
    The alkylation of 4-alkoxymethyl-2-ethoxycarbonylbutanolides led to the formation of 2-alkenyl-4-alkoxymethyl-2-ethoxycarbonylbutanolides which at alkaline hydrolysis provided new 2-alkenyl-4-alkoxymethylbutanolides. By oxidation of the latter with a mixture of hydrogen peroxide and formic acid 4-alkoxymethyl-2-(2-R-2,3-dihydroxy)propylbutanolides were obtained. The diololactones were shown to suffer under the conditions of the pinacol-pinacolone rearrangement a conversion into previously unknown formyl- and epoxylactones.
    DOI:
    10.1134/s1070428006080136
  • 作为产物:
    描述:
    2-allyl-4-propoxymethylbutanolide甲酸双氧水 作用下, 反应 20.0h, 以77%的产率得到2-(2,3-dihydroxy)propyl-4-propoxymethylbutanolide
    参考文献:
    名称:
    Synthesis and some transformations of 2-alkenyl-4-alkoxymethylbutanolides
    摘要:
    The alkylation of 4-alkoxymethyl-2-ethoxycarbonylbutanolides led to the formation of 2-alkenyl-4-alkoxymethyl-2-ethoxycarbonylbutanolides which at alkaline hydrolysis provided new 2-alkenyl-4-alkoxymethylbutanolides. By oxidation of the latter with a mixture of hydrogen peroxide and formic acid 4-alkoxymethyl-2-(2-R-2,3-dihydroxy)propylbutanolides were obtained. The diololactones were shown to suffer under the conditions of the pinacol-pinacolone rearrangement a conversion into previously unknown formyl- and epoxylactones.
    DOI:
    10.1134/s1070428006080136
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