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tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-oxocyclohexa-2,5-dienecarboxylate | 1071817-57-6

中文名称
——
中文别名
——
英文名称
tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-oxocyclohexa-2,5-dienecarboxylate
英文别名
Tert-butyl 2,5-bis(methoxymethoxy)-1-(2-methoxy-2-oxoethyl)-4-oxocyclohexa-2,5-diene-1-carboxylate
tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-oxocyclohexa-2,5-dienecarboxylate化学式
CAS
1071817-57-6
化学式
C18H26O9
mdl
——
分子量
386.399
InChiKey
BNPSOORWHXQVBB-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):
    1.1
  • 重原子数:
    27
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    107
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-oxocyclohexa-2,5-dienecarboxylate2-甲基-1-丁烯-3-炔正丁基锂氯化铵 作用下, 以 乙醚正己烷 为溶剂, 反应 4.0h, 生成 tert-butyl 4-hydroxy-1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-(3-methylbut-3-en-1-ynyl)cyclohexa-2,5-dienecarboxylate
    参考文献:
    名称:
    A Route to 1,4-Disubstituted Aromatics and Its Application to the Synthesis of the Antibiotic Culpin
    摘要:
    A method is described for converting tert-butyl benzoates or tert-butyl 1-naphthoates into derivatives having an alkyl or substituted alkyl group in a 1,4-relationship to an alkyl, aryl, alkenyl, or alkynyl group. Key steps in the sequence are (i) addition of an organometallic species to a cross-conjugated cyclohexadienone obtained by Birch alkylation of a tert-butyl benzoate or a tert-butyl 1-naphthoate, followed by allylic oxidation, and (ii) treatment with BiCl3 center dot H2O, which results in removal of the tertbutyl group and spontaneous decarboxylative aromatization. The method was applied to the synthesis of the antimicrobial fungal metabolite culpin.
    DOI:
    10.1021/jo8015192
  • 作为产物:
    描述:
    tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)cyclohexa-2,5-dienecarboxylate叔丁基过氧化氢重铬酸吡啶 、 Celite 作用下, 以 癸烷 为溶剂, 反应 4.0h, 以72%的产率得到tert-butyl 1-[(methoxycarbonyl)methyl]-2,5-bis(methoxymethoxy)-4-oxocyclohexa-2,5-dienecarboxylate
    参考文献:
    名称:
    A Route to 1,4-Disubstituted Aromatics and Its Application to the Synthesis of the Antibiotic Culpin
    摘要:
    A method is described for converting tert-butyl benzoates or tert-butyl 1-naphthoates into derivatives having an alkyl or substituted alkyl group in a 1,4-relationship to an alkyl, aryl, alkenyl, or alkynyl group. Key steps in the sequence are (i) addition of an organometallic species to a cross-conjugated cyclohexadienone obtained by Birch alkylation of a tert-butyl benzoate or a tert-butyl 1-naphthoate, followed by allylic oxidation, and (ii) treatment with BiCl3 center dot H2O, which results in removal of the tertbutyl group and spontaneous decarboxylative aromatization. The method was applied to the synthesis of the antimicrobial fungal metabolite culpin.
    DOI:
    10.1021/jo8015192
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