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diethyl 2-(1-hydroxyethylidene)malonate | 31575-84-5

中文名称
——
中文别名
——
英文名称
diethyl 2-(1-hydroxyethylidene)malonate
英文别名
(1-hydroxyethylidene)malonic acid diethyl ester;(1-Hydroxy-aethyliden)-malonsaeure-diaethylester;diethyl 2-(1-hydroxyethylidene)propanedioate
diethyl 2-(1-hydroxyethylidene)malonate化学式
CAS
31575-84-5
化学式
C9H14O5
mdl
——
分子量
202.207
InChiKey
QEPNXJHFURABRW-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:
    246.5±40.0 °C(Predicted)
  • 密度:
    1.156±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:1d76dadb314824ba84b3dd4fd90b652d
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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:
    参考文献:
    名称:
    Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones
    摘要:
    The synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones from acylated ethyl acetoacetates and diethyl malonates is described. The reaction of acylated ethyl acetoacetates and diethyl acetylmalonate with hydrazine (98%) gave 3-substituted-pyrazolin-5-ones and malonyidihydrazide, respectively, following a deacetylation-condensation sequence. The reaction of ethyl 2-acetyl-3-hydroxy-2-butenoate and diethyl 2-(1-hydroxyethylidene)malonate with hydrazine monohydrochloride yielded ethyl 3,5-dimethyl-1H-pyrazole-4-carboxylate and 4-ethoxycarbonyl-3-methylpyrazolin-5-one, respectively, following a dehydration-cyclocondensation sequence, in high yields. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)00306-x
  • 作为产物:
    描述:
    乙酰氯丙二酸二乙酯四氯化碳乙醇magnesium 作用下, 以 甲苯四氯化碳乙醇 为溶剂, 反应 2.0h, 以82%的产率得到diethyl 2-(1-hydroxyethylidene)malonate
    参考文献:
    名称:
    Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones
    摘要:
    The synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones from acylated ethyl acetoacetates and diethyl malonates is described. The reaction of acylated ethyl acetoacetates and diethyl acetylmalonate with hydrazine (98%) gave 3-substituted-pyrazolin-5-ones and malonyidihydrazide, respectively, following a deacetylation-condensation sequence. The reaction of ethyl 2-acetyl-3-hydroxy-2-butenoate and diethyl 2-(1-hydroxyethylidene)malonate with hydrazine monohydrochloride yielded ethyl 3,5-dimethyl-1H-pyrazole-4-carboxylate and 4-ethoxycarbonyl-3-methylpyrazolin-5-one, respectively, following a dehydration-cyclocondensation sequence, in high yields. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)00306-x
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文献信息

  • Phase transfer catalyzed acylation
    作者:Volker O. Illi
    DOI:10.1016/s0040-4039(01)86311-5
    日期:1979.1
    Sterically crowded phenols are conveniently acylated under phase transfer conditions. Selective 3-OH acylation of estradiol is accomplished by this method.
    立体上拥挤的苯酚在相转移条件下方便地被酰化。雌二醇的选择性3-OH酰化是通过这种方法完成的。
  • US7514454B2
    申请人:——
    公开号:US7514454B2
    公开(公告)日:2009-04-07
  • Synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones
    作者:Jae-Chul Jung、E.Blake Watkins、Mitchell A Avery
    DOI:10.1016/s0040-4020(02)00306-x
    日期:2002.4
    The synthesis of 3-substituted and 3,4-disubstituted pyrazolin-5-ones from acylated ethyl acetoacetates and diethyl malonates is described. The reaction of acylated ethyl acetoacetates and diethyl acetylmalonate with hydrazine (98%) gave 3-substituted-pyrazolin-5-ones and malonyidihydrazide, respectively, following a deacetylation-condensation sequence. The reaction of ethyl 2-acetyl-3-hydroxy-2-butenoate and diethyl 2-(1-hydroxyethylidene)malonate with hydrazine monohydrochloride yielded ethyl 3,5-dimethyl-1H-pyrazole-4-carboxylate and 4-ethoxycarbonyl-3-methylpyrazolin-5-one, respectively, following a dehydration-cyclocondensation sequence, in high yields. (C) 2002 Elsevier Science Ltd. All rights reserved.
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