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3-甲氧基苯基甲基磷酸氢盐 | 229982-83-6

中文名称
3-甲氧基苯基甲基磷酸氢盐
中文别名
——
英文名称
3-methoxyphenyl methyl hydrogen phosphate
英文别名
3-methoxyphenyl methyl hydrogenphosphate;methyl 3-methoxyphenyl phosphate;(3-Methoxyphenyl) methyl hydrogen phosphate;(3-methoxyphenyl) methyl hydrogen phosphate
3-甲氧基苯基甲基磷酸氢盐化学式
CAS
229982-83-6
化学式
C8H11O5P
mdl
——
分子量
218.146
InChiKey
SPWROUSGUDAHQP-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:
    327.2±44.0 °C(Predicted)
  • 密度:
    1.318±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    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-甲氧基苯基甲基磷酸氢盐 在 palladium(II) trifluoroacetate 、 三甲基硅烷化重氮甲烷 作用下, 以 正己烷1,2-二氯乙烷 为溶剂, 反应 15.5h, 生成 4-methoxy[1,1'-biphenyl]-2-yl dimethyl phosphate
    参考文献:
    名称:
    Pd(II)-Catalyzed ortho-Arylation of Aryl Phosphates and Aryl Hydrogen Phosphates with Diaryliodonium Triflates
    摘要:
    Functionalized biaryl compounds were successfully synthesized using phosphates as the ortho-directing group in the Pd(II)Pd(IV) catalytic cycle.
    DOI:
    10.1021/ol400732q
  • 作为产物:
    描述:
    3-甲氧基苯酚吡啶 、 sodium hydroxide 、 三氯氧磷 作用下, 以 乙醚二氯甲烷 为溶剂, 反应 1.0h, 生成 3-甲氧基苯基甲基磷酸氢盐
    参考文献:
    名称:
    使用新的单磷酸直接基团,钯催化芳基氢磷酸的邻链烯基化。
    摘要:
    首次报道了使用单磷酸定向基团的高效Pd催化的邻链烯基化反应。该磷酸导向基团已成功用于各种烯基化产物的合成,并为过渡金属催化的CH活化提供了一种新方法。
    DOI:
    10.1039/c3cc41107a
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文献信息

  • A Simple DNase Model System Comprising a Dinuclear Zn(II) Complex in Methanol Accelerates the Cleavage of a Series of Methyl Aryl Phosphate Diesters by 10<sup>11</sup>−10<sup>13</sup>
    作者:Alexei A. Neverov、C. Tony Liu、Shannon E. Bunn、David Edwards、Christopher J. White、Stephanie A. Melnychuk、R. Stan Brown
    DOI:10.1021/ja8006963
    日期:2008.5.1
    The di-Zn(II) complex of 1,3-bis[N-1,N-1'-(1,5,9-triazacyclododecyl)] propane with an associated methoxide (3:Zn(II)(2):-OCH3) was prepared and its catalysis of the methanolysis of a series of fourteen methyl aryl phosphate diesters (6) was studied at (s)(s)pH 9.8 in methanol at 25.0 +/- 0.1 degrees C. Plots of k(obs) VS [3:Zn(II)(2):-OCH3](free) for all members of 6 show saturation behavior from which K-M and k(cat)(max) were determined. The second order rate constants for the catalyzed reactions (k(cat)(max)/K-M) for each substrate are larger than the corresponding methoxide catalyzed reaction (k(2)(-OMe)) by 1.4 x 10(8) to 3 x 10(9)-fold. The values of kcatmax for all members of 6 are between 4 x 10(11) and 3 x 10(13) times larger than the solution reaction at (s)(s)pH 9.8, with the largest accelerations being given for substrates where the departing aryloxy unit contains ortho-NO2 or C(= O)OCH3 groups. Based on the linear Bronsted plots of k(cat)(max) VS (s)(s)pK(a)of the phenol, beta(Ig) values of -0.57 and -0.34 are determined respectively for the catalyzed methanolysis of "regular' substrates that do not contain the ortho-NO2 or C(= O)OCH3 groups, and those substrates that do. The data are consistent with a two step mechanism for the catalyzed reaction with rate limiting formation of a catalyst-coordinated phosphorane intermediate, followed by fast loss of the aryloxy leaving group. A detailed energetics calculation indicates that the catalyst binds the transition state comprising [CH3O-:6]double dagger, giving a hypothetical [3:Zn(II)(2):CH3O-:6]double dagger complex, by -21.4 to -24.5 kcal/mol, with the strongest binding being for those substrates having the ortho-NO2 or C(= O)OCH3 groups.
  • <i>ortho</i>-Acetoxylation of Phosphonic and Phosphoric Monoacids via Pd(II) Catalysis
    作者:Li Yan Chan、Xiangjian Meng、Sunggak Kim
    DOI:10.1021/jo4011188
    日期:2013.9.6
    A simple and efficient method is developed for Pd-catalyzed ortho-acetoxylation using organophosphates, namely, benzylic phosphonic and aryl phosphoric monoacids, as the directing group.
  • Palladium-catalyzed ortho-alkenylation of aryl hydrogen phosphates using a new mono-phosphoric acid directing group
    作者:Li Yan Chan、Sunggak Kim、Taekyu Ryu、Phil Ho Lee
    DOI:10.1039/c3cc41107a
    日期:——
    A highly efficient Pd-catalyzed ortho-alkenylation is reported using a mono-phosphoric acid-directing group for the first time. This phosphoric acid-directing group is successfully utilized for the synthesis of various alkenylated products and offers a new approach to transition-metal-catalyzed C-H activation.
    首次报道了使用单磷酸定向基团的高效Pd催化的邻链烯基化反应。该磷酸导向基团已成功用于各种烯基化产物的合成,并为过渡金属催化的CH活化提供了一种新方法。
  • Pd(II)-Catalyzed <i>ortho</i>-Arylation of Aryl Phosphates and Aryl Hydrogen Phosphates with Diaryliodonium Triflates
    作者:Li Yan Chan、Lilian Cheong、Sunggak Kim
    DOI:10.1021/ol400732q
    日期:2013.5.3
    Functionalized biaryl compounds were successfully synthesized using phosphates as the ortho-directing group in the Pd(II)Pd(IV) catalytic cycle.
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