non-1-en-6-ol | 241807-89-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: non-1-en-6-ol
• 英文别名: non-8-en-4-ol；(E)-6-nonen-1-alcohol
• CAS: 241807-89-6
• 化学式: C₉H₁₈O
• 分子量: 142.241
• InChiKey: TVGQDJZFMGWPEO-UHFFFAOYSA-N

物化性质

• 沸点：
  203.1±19.0 °C(Predicted)
• 密度：
  0.836±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  10
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  non-1-en-6-ol 以93%的产率得到non-8-en-4-one
  参考文献：
  名称：

  Nonstabilized N-Unsubstituted Azomethine Ylides:  A Synthesis of Indolizidine 239CD

  摘要：

  [GRAPHICS]Treatment of a (2-azaallyl)stannane with HF . pyridine generated a nonstabilized N-unsubstituted azomethine ylide, which was found to undergo an efficient and stereoselective dipolar cycloaddition with phenyl vinyl sulfone to produce a trans 2,5-dialkylpyrrolidine that was further transformed into the dendrobatid alkaloid indolizidine 239CD.

  DOI：

  10.1021/ol990677v
• 作为产物：
  描述：

  5-己烯-1-醇 以 四氢呋喃 为溶剂， 生成 non-1-en-6-ol
  参考文献：
  名称：

  Nonstabilized N-Unsubstituted Azomethine Ylides:  A Synthesis of Indolizidine 239CD

  摘要：

  [GRAPHICS]Treatment of a (2-azaallyl)stannane with HF . pyridine generated a nonstabilized N-unsubstituted azomethine ylide, which was found to undergo an efficient and stereoselective dipolar cycloaddition with phenyl vinyl sulfone to produce a trans 2,5-dialkylpyrrolidine that was further transformed into the dendrobatid alkaloid indolizidine 239CD.

  DOI：

  10.1021/ol990677v

文献信息

• Intramolecular carbolithiation promoted by a DTBB-catalysed chlorine–lithium exchange
  作者：Miguel Yus、Rosa Ortiz、Fernando F Huerta

  DOI：10.1016/j.tet.2003.09.012

  日期：2003.10

  The reaction of 6-chlorohex-1-ene 1 with lithium powder and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB, 5% molar) in THF at −78°C gives the corresponding organolithium intermediate 2, which by reaction with different electrophiles affords, after hydrolysis with diluted hydrochloric acid, the expected products 3. The same reaction performed at −30°C gives cyclopentyl derivatives 5, probably

  6-氯己-1-烯1与锂粉和催化量的4,4'-二叔丁基联苯（DTBB，5％摩尔）在THF中于-78°C反应，得到相应的有机锂中间体2，通过与不同的亲电试剂反应，经稀盐酸水解后，可提供预期的产物3。在-30℃下进行的相同反应可能通过将开链中间体2环化而得到环状有机锂化合物4，从而得到环戊基衍生物5。当起始材料中的双键包含烷基取代基时，例如化合物6和9，相应的环化被抑制，因此分别获得了相应的无环产物8和11。然而，当在相同位置上的取代基是苯基时，如在原料12和15中一样，分别分离了环化产物14和17。在第二起始氯化物材料18的情况下，该反应可以针对分别在-78或-30℃下工作的无环产物20或环状产物22，如在未取代的情况下发生的那样。氯化物1。对于叔氯衍生物如图23所示，由于相应的叔有机锂中间体24的极大的不稳定性，因此即使在-78℃也仅发生了质子提取，因此在-30℃下仅可以分离环状化合物27。
• Preparation of 1-phenylcyclohexa-2,5-diene-1-carboxylates and their use in free-radical mediated synthesesElectronic supplementary information (ESI) available: experimental procedures for the preparation of 1,4-dihydrobiphenyl,9 1-deuterio-1,4-dihydrobiphenyl, 1-phenylcyclohexa-2,5-diene-1-carboxylic acid with 3,4-dihydrobiphenyl-3-carboxylic acid, 2-(cyclohex-2-enyloxy)ethyl 1-phenylcyclohexa-2,5-diene-1-carboxylate and non-1-en-6-ol. Experimental details of the reactions of cyclopentyl 1-phenylcyclohexa-2,5-diene-1-carboxylate with cyclohexenone, methyl acrylate, methyl methacrylate, acrylonitrile and cyclohexene are included. See http://www.rsc.org/suppdata/p1/b1/b110527m/
  作者：Paul A. Baguley、Leon V. Jackson、John C. Walton

  DOI：10.1039/b110527m

  日期：2002.1.23

  Synthetic routes to pure 1-phenylcyclohexa-2,5-diene-1-carboxylic acid and derived esters were developed. Esters containing appropriately unsaturated side chains generated the corresponding alkenyl radicals and hence gave good yields of 5-exo ring closure products in organotin-free reactions. Extrusion of phenyl radicals from the intermediate cyclohexadienyl type radicals was not observed, and this alternative β-scission did not compete under any conditions. Yields from alkylations of olefins in analogous intermolecular processes were, however, poor. As a spin-off from the research, it was found that 1-phenylcyclohexa-2,5-diene-1-carboxylic acid (6) was a useful source of hydroxyformyl (formate) radicals in organic solvents.

  开发了纯 1-苯基环己-2,5-二烯-1-羧酸及其衍生酯的合成路线。含有适当不饱和侧链的酯类可生成相应的烯基自由基，因此在无有机锡反应中，5-外环闭合产物的产量很高。没有观察到苯基自由基从中间的环己二烯型自由基中挤出，而且这种替代性的 β 分裂在任何条件下都不会产生竞争。不过，在类似的分子间过程中，烯烃烷基化的产量很低。研究的一个附带成果是发现 1-苯基环己-2,5-二烯-1-羧酸（6）是有机溶剂中羟基甲酰（甲酸）自由基的有效来源。
• Method for the preparation of cis-nonen-6-yl chloride
  申请人：Shin-Etsu Chemical Co., Ltd.

  公开号：EP0038053A1

  公开（公告）日：1981-10-21

  The invention provides a novel and efficient method for the synthetic preparation of cis-nonen-6-yl chloride which is a useful intermediate compound for the syntheses of, for example, cis-nonen-6-yl acetate, cis-nonen--6-ol, cis-nonen-6-yl and the like as flavors as well as cis-dodecen-9-yl acetate and cis-tetradecen-11-yl acetate known as sexual pheromone compounds of several noxious insects. The inventive method comprises reacting 1-bromo-3-chloropropane with the Grignard reagent of cis-hexen-3-yl chloride which is a chlorination product of cis-hexen-3-ol known by a trivial name of leaf alcohol. The reaction is preferably carried out in tetrahydrofuran in the presence of a catalyst which may be lithium copper dichloride or dilithium copper tetrachloride at 0 to 40°C.

  本发明提供了一种合成制备顺式壬烯-6-酰氯的新颖而有效的方法，顺式壬烯-6-酰氯是一种有用的中间化合物，可用于合成例如作为香料的顺式壬烯-6-乙酸酯、顺式壬烯-6-醇、顺式壬烯-6-基等，以及作为几种有害昆虫的性信息素化合物的顺式十二烯-9-乙酸酯和顺式十四烯-11-乙酸酯。本发明的方法包括使 1-溴-3-氯丙烷与顺式己烯-3-基氯的格氏试剂反应，顺式己烯-3-基氯是顺式己烯-3-醇的氯化产物，俗称叶醇。反应最好在四氢呋喃中进行，催化剂可以是二氯化铜锂或四氯化二锂铜，温度为 0-40°C 。
• Polar group-containing olefin copolymer, process for preparing the same, thermoplastic resin composition contaning the copolymer, and uses thereof
  申请人：MITSUI CHEMICALS, INC.

  公开号：EP1186619A2

  公开（公告）日：2002-03-13

  The present invention is intended to provide a polar group-containing olefin copolymer having excellent adhesion properties to metals or polar resins and excellent compatibility therewith, a process for preparing the copolymer, a thermoplastic resin composition containing the copolymer, and uses thereof. The polar group-containing olefin copolymer comprises a constituent unit derived from an α-olefin of 2 to 20 carbon atoms, and a constituent unit derived from a straight-chain, branched or cyclic polar group-containing monomer having at the end a polar group such as a hydroxyl group or an epoxy group and/or a constituent unit derived from a macromonomer having at the end a polymer segment obtained by anionic polymerization, ring-opening polymerization or polycondensation. The polar group-containing olefin copolymer can be prepared by polymerizing the α-olefin with the polar group-containing monomer and/or the macromonomer in the presence of a metallocene catalyst. The polar group-containing olefin copolymer and the thermoplastic resin composition containing the copolymer are used for films, sheets, modifiers, building/civil engineering materials, automobile exterior trim, electric/electronic parts, coating bases, compatibilizing agents, etc.

  本发明旨在提供一种对金属或极性树脂具有极佳粘附性和相容性的含极性基团的烯烃共聚物、制备该共聚物的工艺、含有该共聚物的热塑性树脂组合物及其用途。含极性基团的烯烃共聚物包括一个由 2 至 20 个碳原子的 α-烯烃衍生的组成单元和一个由直链、支链或环状含极性基团单体衍生的组成单元，直链、支链或环状含极性基团单体的末端具有极性基团，如羟基或环氧基，和/或一个由大单体衍生的组成单元，大单体的末端具有通过阴离子聚合、开环聚合或缩聚反应获得的聚合物段。含极性基团的烯烃共聚物可通过在茂金属催化剂存在下使α-烯烃与含极性基团的单体和/或大单体聚合来制备。含极性基团的烯烃共聚物和含有该共聚物的热塑性树脂组合物可用于薄膜、板材、改性剂、建筑/土木工程材料、汽车外饰、电气/电子零件、涂层基料、相容剂等。
• Polar group-containing olefin copolymer, process for preparing the same, thermoplastic resin composition containing the copolymer, and uses thereof
  申请人：——

  公开号：US20020156207A1

  公开（公告）日：2002-10-24

  The present invention is intended to provide a polar group-containing olefin copolymer having excellent adhesion properties to metals or polar resins and excellent compatibility therewith, a process for preparing the copolymer, a thermoplastic resin composition containing the copolymer, and uses thereof. The polar group-containing olefin copolymer comprises a constituent unit derived from an &agr;-olefin of 2 to 20 carbon atoms, and a constituent unit derived from a straight-chain, branched or cyclic polar group-containing monomer having at the end a polar group such as a hydroxyl group or an epoxy group and/or a constituent unit derived from a macromonomer having at the end a polymer segment obtained by anionic polymerization, ring-opening polymerization or polycondensation. The polar group-containing olefin copolymer can be prepared by polymerizing the &agr;-olefin with the polar group-containing monomer and/or the macromonomer in the presence of a metallocene catalyst. The polar group-containing olefin copolymer and the thermoplastic resin composition containing the copolymer are used for films, sheets, modifiers, building/civil engineering materials, automobile exterior trim, electric/electronic parts, coating bases, compatibilizing agents, etc.

  本发明旨在提供一种对金属或极性树脂具有极佳粘附性能和极佳相容性的含极性基团的烯烃共聚物、制备该共聚物的工艺、含有该共聚物的热塑性树脂组合物及其用途。含极性基团的烯烃共聚物包括一个由 2 至 20 个碳原子的&agr;-烯烃衍生的组成单元，以及一个由直链、支链或环状含极性基团单体衍生的组成单元，该单体末端具有极性基团，如羟基或环氧基，和/或一个由大单体衍生的组成单元，该大单体末端具有通过阴离子聚合、开环聚合或缩聚反应获得的聚合物段。含极性基团的烯烃共聚物可通过在茂金属催化剂存在下，将&agr;-烯烃与含极性基团的单体和/或大单体进行聚合来制备。含极性基团的烯烃共聚物和含有该共聚物的热塑性树脂组合物可用于薄膜、板材、改性剂、建筑/土木工程材料、汽车外饰、电气/电子零件、涂层基料、相容剂等。