butanoyl succinate de methyle | 68245-81-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 酮酸及其衍生物
• 英文名称: butanoyl succinate de methyle
• 英文别名: 2-butyrylsuccinic acid dimethyl ester；dimethyl 2-butanoylbutanedioate；dimethyl 2-butyrylsuccinate；Butyryl-bernsteinsaeure-dimethylester；(1-oxo-butyl)-butanedioic acid dimethyl ester；butyryl-succinic acid dimethyl ester
• CAS: 68245-81-8
• 化学式: C₁₀H₁₆O₅
• 分子量: 216.234
• InChiKey: CMGBZGKUSJAGHU-UHFFFAOYSA-N

物化性质

• 熔点：
  26 °C
• 沸点：
  142-145 °C(Press: 5 Torr)
• 密度：
  1.091±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  15
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.7
• 拓扑面积：
  69.7
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  butanoyl succinate de methyle 在 水 、 lithium hydroxide 作用下， 以 水 为溶剂， 生成 乙酰丙酸
  参考文献：
  名称：

  Total Synthesis and Evaluation of a Key Series of C5-Substituted Vinblastine Derivatives

  摘要：

  A remarkably concise seven- to eight-step total synthesis of a systematic series of key vinblastine derivatives is detailed and used to characterize the importance and probe the role of the C5 ethyl substituent (R = H, Me, Pr, CH=CH(2), C CH, CH(2)OH, and CHO vs Et). The analogues, which bear deep-seated structural changes accessible only by total synthesis, were prepared using a powerful intramolecular [4 + 2]/[3 + 2] cycloaddition cascade of 1,3,4-oxadiazoles ideally suited for use in the assemblage of the vindoline-derived lower subunit followed by their incorporation into the vinblastine analogues through the use of a single-step biomimetic coupling with catharanthine. The evaluation of the series revealed that the tubulin binding site surrounding this C5 substituent is exquisitely sensitive to the presence (Et > H, 10-fold), size (Me <= Et > Pr, 10-fold), shape (Et > CH=CH(2) and C CH, >4-fold), and polarity (Et > CHO > CH(2)OH, >10-20-fold) of this substituent and that on selected occasions only a C5 methyl group may provide analogues that approach the activity observed with the naturally occurring C5 ethyl group.

  DOI：

  10.1021/ja1027748
• 作为产物：
  描述：

  正丁醛 、 1,4-dimethyl but-2-enedioate 以 1,4-二氧六环 为溶剂， 反应 72.0h， 以70%的产率得到butanoyl succinate de methyle
  参考文献：
  名称：

  Metal-free, hydroacylation of CC and NN bonds via aerobic C–H activation of aldehydes, and reaction of the products thereof

  摘要：

  在本报告中，我们详细评估了使用需氧起始、不含金属的氢酰化方法，将多种CC和NN受体分子与广泛范围的醛进行反应的情况。我们所开发的有氧活化条件与之前的氢酰化条件形成鲜明对比，后者倾向于使用过渡金属、需要热或光化学分解的过氧化物，或者N-杂环卡宾。这些温和的条件使得许多涉及敏感反应物的反应得以进行，或许最为重要的是，能够让α-功能化的手性醛在基于自由基的氢酰化反应中完全保持光学纯度。我们还展示了所得氢酰化产物如何转化成其他有用的中间体，例如γ-酮-磺酰胺、磺内酰胺、磺内酯、环状N-磺酰亚胺和酰胺。

  DOI：

  10.1039/c3ob41632a

文献信息

• Hydroacylation of α,β-unsaturated esters via aerobic C–H activation
  作者：Vijay Chudasama、Richard J. Fitzmaurice、Stephen Caddick

  DOI：10.1038/nchem.685

  日期：2010.7

  using selective C–H activation as a direct route for generating reactive intermediates. In this article, we describe the use of aldehyde auto-oxidation as a simple, clean and effective method for C–H activation, resulting in the generation of an acyl radical. This acyl radical can be used for carbon–carbon bond formation and herein we describe the application of this method for the hydroacylation of α

  开发在良性条件下形成碳-碳键的方法对合成化学家来说是一个持续的挑战。近年来，人们对使用选择性 C-H 活化作为生成活性中间体的直接途径产生了相当大的兴趣。在本文中，我们描述了使用醛自动氧化作为一种​​简单、清洁和有效的 C-H 活化方法，从而产生酰基自由基。这种酰基自由基可用于碳-碳键的形成，在此我们描述了这种方法在 α,β-不饱和酯的加氢酰化中的应用，而不需要额外的催化剂或试剂。这种方法产生不对称的酮，已被证明在有机合成中具有广泛的用途。
• [EN] ALICYCLIC MUSK FRAGRANCE COMPOUNDS<br/>[FR] COMPOSÉS ALICYCLIQUES DE PARFUM MUSQUÉ
  申请人：SYMRISE AG

  公开号：WO2020125993A1

  公开（公告）日：2020-06-25

  The present invention primarily relates to the use of a compound according to the general formula (I) wherein i) m is 1, n is 1, o is 0 or 1, Y is Hydrogen, or ii) m is 2, n is 0, o is 1, Y is methyl, and wherein X is O or methylene, R and R1 are each methyl or form together with the carbon atom attached to a carbonyl group, and R2 is methyl, ethyl, propyl, butyl, butan-2-one-4-yl, tetrahydrofuran-2-yl, or tetrahydrofuran-3-yl, as perfuming ingredients. Moreover, the present invention relates to perfume compositions and perfumed products comprising the before mentioned perfuming ingredients. Still more particularly, the invention relates to a method for producing said perfumed products and a method of imparting and/or increasing musk odor characteristics to perfumed products. This invention also relates to a process for the preparation of said compounds according to the general formula (I).

  本发明主要涉及使用符合一般式(I)的化合物，其中i）m为1，n为1，o为0或1，Y为氢，或ii）m为2，n为0，o为1，Y为甲基，X为O或亚甲基，R和R1分别为甲基或与连接到羰基的碳原子形成一起的，R2为甲基、乙基、丙基、丁基、丁酮-2-基、四氢呋喃-2-基或四氢呋喃-3-基，作为香料成分。此外，本发明涉及包含上述香料成分的香水组合物和带有香水成分的香水产品。更具体地，本发明涉及生产所述香水产品的方法以及赋予和/或增加香水产品的麝香气味特征的方法。本发明还涉及根据一般式(I)制备所述化合物的方法。
• Efficient C(sp³)−H Carbonylation of Light and Heavy Hydrocarbons with Carbon Monoxide via Hydrogen Atom Transfer Photocatalysis in Flow**
  作者：Fabian Raymenants、Tom M. Masson、Jesús Sanjosé‐Orduna、Timothy Noël

  DOI：10.1002/anie.202308563

  日期：2023.9.4

  an efficient C−H functionalization process, enabling the regioselective installation of carbonyls in light and heavy hydrocarbons by using inexpensive carbon monoxide. Safe processing of hazardous CO and flammable alkanes is ensured in flow, with high gas-liquid mass transfer rates and fast reaction kinetics. Our method demonstrates the valorization of gaseous reagents, coupling light alkanes, CO, and

  我们报告了一种高效的 C−H 官能化过程，通过使用廉价的一氧化碳，能够在轻质和重质烃中选择性安装羰基。具有高气液传质速率和快速反应动力学，可确保危险的 CO 和易燃烷烃的安全加工。我们的方法演示了气态试剂的增值，将轻质烷烃、CO 和烯烃偶联作为末端自由基陷阱。
• A convenient route to chiral γ-lactones via asymmetric hydrogenation of γ-ketoesters using the RuCl3–BINAP–HCl catalytic system
  作者：Eugenia V. Starodubtseva、Olga V. Turova、Maxim G. Vinogradov、Lilia S. Gorshkova、Vladimir A. Ferapontov、Marina I. Struchkova

  DOI：10.1016/j.tet.2008.10.012

  日期：2008.12

  A convenient one-step synthesis of chiral gamma-lactones has been performed. The method is based on enantioselective hydrogenation of gamma-ketoesters using the RuCl3-BINAP-HCl catalytic system. Chiral gamma-lactones (91-99% ee) have been isolated in 57-88% yield. (C) 2008 Elsevier Ltd. All rights reserved.
• Bouveault; Bongert, Bulletin de la Societe Chimique de France, 1902, vol. <3> 27, p. 1083,1088, 1089
  作者：Bouveault、Bongert

  DOI：——

  日期：——