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(Z)-3-Methyl-oct-2-enoic acid methyl ester

中文名称
——
中文别名
——
英文名称
(Z)-3-Methyl-oct-2-enoic acid methyl ester
英文别名
Methyl 3-methyloct-2-enoate;methyl 3-methyloct-2-enoate
(Z)-3-Methyl-oct-2-enoic acid methyl ester化学式
CAS
——
化学式
C10H18O2
mdl
——
分子量
170.252
InChiKey
RNZCYKUDIMXQCI-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):
    3.6
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    (Z)-3-Methyl-oct-2-enoic acid methyl esterplatinum(IV) oxide lithium aluminium tetrahydride 、 氢气magnesium 、 lithium bromide 作用下, 以 吡啶甲醇乙醚丙酮 为溶剂, 100.0 ℃ 、10.13 MPa 条件下, 反应 25.5h, 生成 4-methylnonan-1-ol
    参考文献:
    名称:
    Carpita, Adriano; Magistris, Elisabetta De; Rossi, Renzo, Gazzetta Chimica Italiana, 1989, vol. 119, # 2, p. 99 - 106
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-Diazo-3-methyl-octanoic acid methyl ester 在 rhodium(II) acetate dimer 作用下, 生成 (Z)-3-Methyl-oct-2-enoic acid methyl ester
    参考文献:
    名称:
    Rhodium-mediated cyclopentane construction can compete with .beta.-hydride elimination: synthesis of (.+-.)-tochuinyl acetate
    摘要:
    Rhodium(II) carboxylate catalyzed C-H insertion to form a cyclopentane is shown to compete effectively with beta-hydride elimination, except when the beta-hydrogen is ternary. Cyclization of diazo ester 27 gives 28, which is converted in three steps to (+/-)-tochuinyl acetate 25. Both the cyclization to form 28 and the alkylation of 28 proceed with remarkable diastereoselectivity.
    DOI:
    10.1021/jo00028a011
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文献信息

  • 4-<i>Endo</i>-<i>T</i><i>rig</i> Cyclization Processes Using Bis(collidine)bromine(I) Hexafluorophosphate as Reagent:  Preparation of 2-Oxetanones, 2-Azetidinones, and Oxetanes
    作者:Fadi Homsi、Gérard Rousseau
    DOI:10.1021/jo9810361
    日期:1999.1.1
    Reaction in methylene chloride of bis(collidine)bromine(I) hexafluorophosphate with alpha,beta-unsaturated acids and alpha,beta-unsaturated N-sulfonamides was found to lead diastereospecifically to the corresponding 2-oxetanones and 2-azetidinones in moderate yields (23-60%), by an almost unknown 4-endo cyclization. This process allow the synthesis of these interesting classes of products in one step
    发现六氟磷酸双(可力丁)溴(I)在二氯甲烷中与α,β-不饱和酸和α,β-不饱和N-磺酰胺的反应以中等收率非对映特异性地导致相应的2-氧杂环丁烷和2-氮杂环丁烷酮(23 -60%),几乎是未知的4内环化。该方法允许一步一步从普通底物合成这些有趣的产品类别。类似地,肉桂醇的反应通过相同的环化步骤导致了氧杂环丁烷(20-36%);在醇官能团的α中存在宝石-二甲基基团似乎是有益的。
  • A new procedure for Horner-Wadsworth-Emmons olefination of carbonyl compounds
    作者:Francesco Bonadies、Antonella Cardilli、Alessandra Lattanzi、Liliana R. Orelli、Arrigo Scettri
    DOI:10.1016/s0040-4039(00)76914-0
    日期:1994.5
    aldehydes undergo an efficient E-stereoselective Horner-Wadsworth-Emmons olefination by generation of phosphonate carbanion with lithium hydroxide. The reaction proceeds satisfactorily with linear, cyclic, polifunctional ketones in the presence of activated zeolites and and by the slow addition of the base.
    醛通过与氢氧化锂生成膦酸酯碳负离子而进行有效的E-立体选择性Horner-Wadsworth-Emmons烯化反应。在活化沸石的存在下,并通过缓慢添加碱,该反应可令人满意地用线性,环状,多官能酮进行。
  • Carpita, Adriano; Magistris, Elisabetta De; Rossi, Renzo, Gazzetta Chimica Italiana, 1989, vol. 119, # 2, p. 99 - 106
    作者:Carpita, Adriano、Magistris, Elisabetta De、Rossi, Renzo
    DOI:——
    日期:——
  • Rhodium-mediated cyclopentane construction can compete with .beta.-hydride elimination: synthesis of (.+-.)-tochuinyl acetate
    作者:Douglass F. Taber、Michael J. Hennessy、James P. Louey
    DOI:10.1021/jo00028a011
    日期:1992.1
    Rhodium(II) carboxylate catalyzed C-H insertion to form a cyclopentane is shown to compete effectively with beta-hydride elimination, except when the beta-hydrogen is ternary. Cyclization of diazo ester 27 gives 28, which is converted in three steps to (+/-)-tochuinyl acetate 25. Both the cyclization to form 28 and the alkylation of 28 proceed with remarkable diastereoselectivity.
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