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2,2-dimethyl-5,5-bis-(3-methyl-2-methylene-but-3-enyl)-[1,3]dioxane-4,6-dione

中文名称
——
中文别名
——
英文名称
2,2-dimethyl-5,5-bis-(3-methyl-2-methylene-but-3-enyl)-[1,3]dioxane-4,6-dione
英文别名
2,2-Dimethyl-5,5-bis(3-methyl-2-methylidenebut-3-enyl)-1,3-dioxane-4,6-dione;2,2-dimethyl-5,5-bis(3-methyl-2-methylidenebut-3-enyl)-1,3-dioxane-4,6-dione
2,2-dimethyl-5,5-bis-(3-methyl-2-methylene-but-3-enyl)-[1,3]dioxane-4,6-dione化学式
CAS
——
化学式
C18H24O4
mdl
——
分子量
304.386
InChiKey
JDOIFWWBCZIEMA-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):
    6
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    N-甲基马来酰亚胺2,2-dimethyl-5,5-bis-(3-methyl-2-methylene-but-3-enyl)-[1,3]dioxane-4,6-dione四氢呋喃 为溶剂, 反应 18.0h, 以64%的产率得到2,2-dimethyl-5,5-bis-(2,6-dimethyl-1,3-dioxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-5-ylmethyl)-[1,3]-dioxane-4,6-dione
    参考文献:
    名称:
    Palladium catalysed reactions of allene with active methylene pronucleophiles. C-1,3-Dienylmethyl derivatives and their Diels–Alder reactions
    摘要:
    A 2-step 100% atom economic sequence is reported whereby active methylene pronucleophiles react with 2 mol equiv. of allene to give bis-1,3-dienylmethyl derivatives of the pronucleophiles. Subsequent double Diels-Alder reactions furnish 1,1'-linked cyclohexenes with a 3-carbon spacer. (C) 2001 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(01)00924-3
  • 作为产物:
    描述:
    丙二酸环(亚)异丙酯丙二烯四(三苯基膦)钯 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以61%的产率得到2,2-dimethyl-5,5-bis-(3-methyl-2-methylene-but-3-enyl)-[1,3]dioxane-4,6-dione
    参考文献:
    名称:
    Palladium catalysed reactions of allene with active methylene pronucleophiles. C-1,3-Dienylmethyl derivatives and their Diels–Alder reactions
    摘要:
    A 2-step 100% atom economic sequence is reported whereby active methylene pronucleophiles react with 2 mol equiv. of allene to give bis-1,3-dienylmethyl derivatives of the pronucleophiles. Subsequent double Diels-Alder reactions furnish 1,1'-linked cyclohexenes with a 3-carbon spacer. (C) 2001 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(01)00924-3
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文献信息

  • Palladium catalysed reactions of allene with active methylene pronucleophiles. C-1,3-Dienylmethyl derivatives and their Diels–Alder reactions
    作者:Ronald Grigg、Ngampong Kongathip、Boonsang Kongathip、Suwaporn Luangkamin、H.Ali Dondas
    DOI:10.1016/s0040-4020(01)00924-3
    日期:2001.10
    A 2-step 100% atom economic sequence is reported whereby active methylene pronucleophiles react with 2 mol equiv. of allene to give bis-1,3-dienylmethyl derivatives of the pronucleophiles. Subsequent double Diels-Alder reactions furnish 1,1'-linked cyclohexenes with a 3-carbon spacer. (C) 2001 Published by Elsevier Science Ltd.
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