反-5-辛烯醛 | 41547-29-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 反-5-辛烯醛
• 英文名称: trans-oct-5-enal
• 英文别名: (5E)-octenal；trans-5-octenal；oct-5t-enal；oct-3-en-8-one；5E-octenal；5-Octenal；(E)-oct-5-enal
• CAS: 41547-29-9
• 化学式: C₈H₁₄O
• 分子量: 126.199
• InChiKey: ZUSUVEKHEZURSD-ONEGZZNKSA-N

物化性质

• 沸点：
  172.9±19.0 °C(Predicted)
• 密度：
  0.832±0.06 g/cm3(Predicted)
• LogP：
  2.512 (est)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  9
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

安全信息

• WGK Germany：
  3

反应信息

• 作为反应物：
  描述：

  反-5-辛烯醛 在 N-氯代丁二酰亚胺 、 L-脯氨酸 作用下， 以 二氯甲烷 为溶剂， 以37%的产率得到(5E)-2-chloro-5-octenal
  参考文献：
  名称：

  A General Strategy for the Stereocontrolled Preparation of Diverse 8- and 9-Membered Laurencia-Type Bromoethers

  摘要：

  A unique procedure to effect a ring-expanding bromoetherification process is described, wherein tetrahydrofurans and tetrahydropyrans are smoothly transformed into 8- and 9-membered bromoethers in a regio- and stereocontrolled manner through the use of BDSB (bromodiethylsulfonium bromopentachloroantimonate). These products resemble the cores of the Laurencia C15 acetogenins. In light of the generality and effectiveness of the approach, this work provides a unique strategy for their laboratory preparation and may implicate a possible biosynthesis pathway.

  DOI：

  10.1021/ja2069449
• 作为产物：
  描述：

  oct-5t-enenitrile 在 二异丁基氢化铝 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 1.5h， 以1.26 g的产率得到反-5-辛烯醛
  参考文献：
  名称：

  A General Strategy for the Stereocontrolled Preparation of Diverse 8- and 9-Membered Laurencia-Type Bromoethers

  摘要：

  A unique procedure to effect a ring-expanding bromoetherification process is described, wherein tetrahydrofurans and tetrahydropyrans are smoothly transformed into 8- and 9-membered bromoethers in a regio- and stereocontrolled manner through the use of BDSB (bromodiethylsulfonium bromopentachloroantimonate). These products resemble the cores of the Laurencia C15 acetogenins. In light of the generality and effectiveness of the approach, this work provides a unique strategy for their laboratory preparation and may implicate a possible biosynthesis pathway.

  DOI：

  10.1021/ja2069449

文献信息

• [EN] ENOL ETHER PROPERFUME<br/>[FR] PRO-PARFUM D'ÉTHER ÉNOLIQUE
  申请人：FIRMENICH & CIE

  公开号：WO2021250164A1

  公开（公告）日：2021-12-16

  The present invention relates to compounds of formula (I) as properfume compounds. In particular, the present invention relates to a method to release a compound being a carbonyl of formula (II), a formate ester of formula (III) and/or an alcohol of formula (IV), by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, the present invention relates to a perfuming composition and a perfumed consumer product comprising at least one compound of formula (I).

  本发明涉及作为合适香精化合物的公式(I)的化合物。具体而言，本发明涉及一种释放公式(I)化合物的方法，该方法是通过将公式(I)化合物暴露在氧化环境中，释放出公式(II)的醛基、公式(III)的甲酸酯基和/或公式(IV)的醇基。此外，本发明涉及一种香精组合物和一种含有至少一种公式(I)化合物的香精消费产品。
• Improved Cope-type hydroamination reactivity of hydrazine derivatives
  作者：Francis Loiseau、Christian Clavette、Michaël Raymond、Jean-Grégoire Roveda、Alishya Burrell、André M. Beauchemin

  DOI：10.1039/c0cc02403a

  日期：——

  A systematic investigation on the metal-free, Cope-type hydroamination reactivity of hydrazides and analogues is reported. Optimization of the hydrazide structure resulted in more facile intramolecular reactivity and enabled intermolecular reactions of alkenes, thus providing a direct approach to polysubstituted hydrazides.

  报道了对无金属、Cope型偶氮胺反应性的肼羧酸及其类似物的系统研究。优化肼羧酸结构使分子内反应更加容易，并实现了烯烃的分子间反应，从而提供了一种直接制备多取代肼羧酸的方法。
• New sigmatropic sequences based on the [2,3]-wittig rearrangement of the bis-allylic ether system
  作者：Kōichi Mikami、Naoyuki Kishi、Takeshi Nakai、Yoshiji Fujita

  DOI：10.1016/s0040-4020(01)90580-0

  日期：1986.1

  Four new sigmatropic sequences triggered by the regiocontrolled [2,3]-Wittig rearrangement of unsymmetrical bis-allylic ethers (1) to the l,5-dien-3-ols (2) arc described, which provide unique, regiocontrolled methods for the synthesis of a wide variety of unsaturated carbonyl compounds possessing interesting molecular frameworks. The newly developed sequences include the [2,3]-Wittig-Claisen, the

  描述了由不对称双烯丙基醚（1）到1,5-二烯-3-醇（2）的区域控制[2,3] -Wittig重排触发的四个新的sigmatropic序列，它们提供了独特的区域控制方法具有令人感兴趣的分子框架的各种不饱和羰基化合物的合成。新开发的序列包括[2,3] -Wittig-Claisen，串联[2,3] -Wittig-oxy-Cope，串联oxy-Cope-Claisen和串联oxy-Cope-Cope序列。
• APPLICATIONS OF THE TANDEM [2,3]-WITTIG-OXY-COPE REARRANGEMENT TO SYNTHESES OF<i>exo</i>-BREVICOMIN AND OXOCRINOL. THE SCOPE AND LIMITATION OF THE SIGMATROPIC SEQUENCES AS A SYNTHETIC METHOD FOR δ,ε-UNSATURATED KETONES
  作者：Koichi Mikami、Takeshi Nakai

  DOI：10.1246/cl.1982.1349

  日期：1982.9.5

  The synthetic utility of the title sigmatropic sequence is illustrated in the syntheses of E-6-nonen-2-one, a precursor of exo-brevicomin, and oxocrinol. The scope and limitation of this sequence as a synthetic method for δ,e-unsaturated ketones are also discussed.

  标题 sigmatropic 序列的合成效用在 E-6-nonen-2-one、exo-brevicomin 的前体和 oxocrinol 的合成中得到了说明。还讨论了该序列作为 δ,e-不饱和酮的合成方法的范围和限制。
• Synthese der vier stereoisomeren Dihydropalustraminsäuren. 13. Mitteilung über Schachtelhalmalkaloide
  作者：Peter Christian Wálchli、Conrad Hans Eugster

  DOI：10.1002/hlca.19780610236

  日期：1978.3.8

  Syntheses of the four stereoisomeric dihydropalustramic acids ([6-(1-hydroxypropyl)-2-piperidyl]acetic acids)

  四种立体异构体的二氢palustramic酸（[6-（1-羟丙基）-2-哌啶基]乙酸）的合成