1-乙酰氧基-1-环己基-2-丁烯 | 163181-69-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 1-乙酰氧基-1-环己基-2-丁烯
• 英文名称: 1-Acetoxy-1-cyclohexyl-2-butene
• 英文别名: (+/-)-acetic acid-(1-cyclohexyl-but-2t-enyl ester)；(+/-)-Essigsaeure-(1-cyclohexyl-but-2t-enylester)；[(E)-1-cyclohexylbut-2-enyl] acetate
• CAS: 163181-69-9
• 化学式: C₁₂H₂₀O₂
• 分子量: 196.29
• InChiKey: IVFLZHPXQFTFIE-XVNBXDOJSA-N

物化性质

• 沸点：
  262.3±9.0 °C(Predicted)
• 密度：
  0.956±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-乙酰氧基-1-环己基-2-丁烯 生成 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  Some Structural and Geometric Isomers of 1-Cyclohexyl-1,3-butadiene¹

  摘要：

  DOI：

  10.1021/ja01586a048
• 作为产物：
  描述：

  1-环己基-2-丁烯醇 、 乙酸酐 在 吡啶 作用下， 生成 1-乙酰氧基-1-环己基-2-丁烯
  参考文献：
  名称：

  Some Structural and Geometric Isomers of 1-Cyclohexyl-1,3-butadiene¹

  摘要：

  DOI：

  10.1021/ja01586a048

文献信息

• Molybdenum(II)- and Tungsten(II)-Catalyzed Allylic Substitution
  作者：Andrei V. Malkov、Ian R. Baxendale、Dalimil Dvořák、Darren J. Mansfield、Pavel Kočovský

  DOI：10.1021/jo9821776

  日期：1999.4.1

  The molybdenum(II) complexes Mo(CO)(5)(OTf)(2) (7a), [Mo(CO)(4)Br(2)](2) (8a), their tungsten(II) congeners 7b and 8b, and bimetallic complex Mo(CO)(3)(MeCN)(2)(SnCl(3))Cl (9a) have been found to catalyze the C-C bond-forming allylic substitution with silyl enol ethers derived from beta-dicarbonyls (e.g., 16 + 30 --> 46) or from simple ketones (e.g., 16 + 32 --> 50), aldehydes, and esters as nucleophiles

  钼（II）络合物Mo（CO）（5）（OTf）（2）（7a），[Mo（CO）（4）Br（2）]（2）（8a），它们的钨（II）同系物7b和8b，发现双金属配合物Mo（CO）（3）（MeCN）（2）（SnCl（3））Cl（9a）可以催化衍生自β-二羰基的甲硅烷基烯醇醚形成CC键的烯丙基取代（例如16 + 30-> 46）或简单的酮（例如16 + 32-> 50），醛和酯在温和的条件下（室温，1-2小时）作为亲核试剂。甲醇作为原型氧亲核试剂，以相似的方式反应（例如16 + MeOH-> 43）。机械和立体化学实验表明路易斯酸催化而不是金属模板控制的过程。
• Cobalt(II) chloride catalysed conversion of allylic alcohols to rearranged allylic amides
  作者：Naresh K. Nayyar、M. Madhava Reddy、Javed Iqbal

  DOI：10.1016/0040-4039(91)80456-g

  日期：1991.11

  Secondary and tertiary allylic alcohols can be converted to the corresponding allylically rearranged amides and acetates in presence of a catalytic quantity of cobalt(II) chloride and acetic anhydride in acetonitrile. Tertiary alcohols undergo complete rearrangement whereas the secondary ones yield a mixture of regioisomers.

  可以在催化量的氯化钴（II）和乙酸酐在乙腈中存在的情况下，将仲和叔烯丙基醇转化为相应的烯丙基重排的酰胺和乙酸酯。叔醇进行完全重排，而仲醇产生区域异构体的混合物。
• Cobalt catalyzed regioselective allylation of 1,3-dicarbonyl compounds
  作者：Golak C. Maikap、M. Madhava Reddy、Manoj Mukhopadhyay、Beena Bhatia、Javed Iqbal

  DOI：10.1016/s0040-4020(01)85380-1

  日期：1994.1

  Catalytic amount of Cobalt(II) chloride in 1,2-dichloroethane promotes the allylation of 1,3-dicarbonyl compounds with allyl acetates in high yields. The allylation of pentane-2,4-dione is highly regioselective as compared with methylacetoacetate and ethyl 2-oxocyclopentanecarboxylate.

  催化量的1,2-二氯乙烷中的氯化钴（II）以高收率促进1,3-二羰基化合物与乙酸烯丙酯的烯丙基化。与乙酰乙酸甲酯和2-氧代环戊烷甲酸乙酯相比，戊烷-2,4-二酮的烯丙基化具有高度的区域选择性。
• Cobalt(II)-Catalyzed Conversion of Allylic Alcohols/Acetates to Allylic Amides in the Presence of Nitriles
  作者：Manoj Mukhopadhyay、M. Madhava Reddy、G. C. Maikap、Javed Iqbal

  DOI：10.1021/jo00114a013

  日期：1995.5

  Various secondary allylic alcohols or their acetates and tertiary allylic alcohols can be converted to the corresponding transposed allylic amides in the presence of a catalytic quantity of cobalt(II) chloride and acetic anhydride in acetonitrile. Tertiary alcohols undergo complete rearrangement whereas secondary ones afford a mixture of regioisomers. Moderate yields of amides are also obtained by reacting acrylonitrile with secondary alcohols in 1,2-dichloroethane. The presence of acetic anhydride or acetic acid is crucial to the formation of amides as the absence of the former affords no amides and the allylic alcohols are mainly recovered as regioisomeric mixtures. The regioselectivity during amide formation can be enhanced by using cobalt complexes 14-16 in acetic acid medium. Some preliminary studies indicate that these reactions are proceeding via an pi-allyl complex or tight ion pair rather than a [3,3] sigmatropic rearrangement of acetamidate obtained in a Pinner reaction.
• Kinetic resolution of racemic allylic acetates by asymmetric dihydroxylation (ADH) process: An indication of π-π interaction
  作者：Braj B. Lohray、Vidya Bhushan

  DOI：10.1016/s0040-4039(00)79261-6

  日期：1993.6

  Kinetic resolution of several racemic secondary allylic acetates have been examined using osmium tetroxide-cinchona alkaloid as chiral catalyst. The unexpected results have been rationalized with the help of model based on pi-pi interaction in the transition state apart from the matching and mismatching of the substrate and the catalyst.