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(2E,4E,6E)-1-diethoxyphosphoryl-3,7,11-trimethyldodeca-2,4,6,10-tetraene

中文名称
——
中文别名
——
英文名称
(2E,4E,6E)-1-diethoxyphosphoryl-3,7,11-trimethyldodeca-2,4,6,10-tetraene
英文别名
——
(2E,4E,6E)-1-diethoxyphosphoryl-3,7,11-trimethyldodeca-2,4,6,10-tetraene化学式
CAS
——
化学式
C19H33O3P
mdl
——
分子量
340.4
InChiKey
YNMLATISXLVFAD-RXBZWHJBSA-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):
    5.5
  • 重原子数:
    23
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • 1,4,6,10-Tetra-Double Bond Pentadec-Carbon Phosphonate, Preparation Method Thereof, And Preparation Method Of Lycopene Using The Same
    申请人:Shen Runpu
    公开号:US20120310002A1
    公开(公告)日:2012-12-06
    1,4,6,10-tetra-double bond pentadec-carbon phosphonate of formula (4), and preparation method thereof are provided. The preparation method comprises: reacting a pseudo ionone of formula (2) with sulfonium salt to prepare a epoxide of formula (9), and then reacting the epoxide of formula (9) with magnesium bromide to prepare a C-14 aldehyde of formula (3); condensing the C-14 aldehyde of formula (3) with tetra-alkyl methylene diphosphonate to obtain 1,4,6,10-tetra-double bond pentadec-carbon phosphonate of formula (4). Furthermore, the preparation method of lycopene via 1,4,6,10-tetra-double bond pentadec-carbon phosphonate of formula (4) is also provided. The present method has the advantages of short route, easily obtained raw materials, and low cost.
    提供了一种化学式为(4)的1,4,6,10-四双键十五碳膦酸酯及其制备方法。制备方法包括:将化学式为(2)的伪离子酮与硫銨盐反应制备出化学式为(9)的环氧化物,然后将化学式为(9)的环氧化物与溴化镁反应制备出化学式为(3)的C-14醛;将化学式为(3)的C-14醛与四烷基亚甲基二膦酸酯进行缩合反应得到化学式为(4)的1,4,6,10-四双键十五碳膦酸酯。此外,还提供了通过化学式为(4)的1,4,6,10-四双键十五碳膦酸酯制备番茄红素的制备方法。该方法具有路线短、原料易得、成本低的优点。
  • INTERMEDIATE OF LYCOPENE AND PREPARATION METHOD OF INTERMEDIATE
    申请人:Zhaoxing University
    公开号:US20140005442A1
    公开(公告)日:2014-01-02
    The present invention relates to 2,6,10-trimethyl-3,5,9-undecatrienyl-1-aldehyde represented by formula (3), and a method for preparing this intermediate. The process route of the present invention is simple, the starting materials are available easily, and the cost is low.
    本发明涉及由化学式(3)表示的2,6,10-三甲基-3,5,9-十一烯基-1-醛,以及制备该中间体的方法。本发明的工艺路线简单,起始材料易获得,成本低。
  • 1-Methoxyl-2, 6, 10-Trimethyl-1, 3, 5, 9-Undec-Tetraene, and Preparation Method and Uses thereof
    申请人:Lao Xuejun
    公开号:US20130046114A1
    公开(公告)日:2013-02-21
    The invention discloses an intermediate 1-methoxyl-2,6,10-trimethyl-1,3,5,9-undec-tetraene, and a preparation method and uses thereof. In the synthesis method for the current lycopene intermediate 2-pos double bond C-14 aldehyde (2,6,10-trimethyl-2,5,9-undecatriene-1-aldehyde), expensive methyl iodide, polluting dimethyl sulphide and dangerous strong base are needed, so that the method is hardly applied to industrial production. The invention provides a new compound 1-methoxyl-2,6,10-trimethyl-1,3,5,9-undec-tetraene, and pure 2-pos double bond C-14 aldehyde can be prepared by hydrolyzing and refining the compound. The synthetic route is simplified and the great suitability for industrial production is achieved.
    该发明公开了一种中间体1-甲氧基-2,6,10-三甲基-1,3,5,9-十一烯,以及其制备方法和用途。在当前番茄红素中间体2-位置双键C-14醛(2,6,10-三甲基-2,5,9-十一烯-1-醛)的合成方法中,需要昂贵的碘甲烷、污染性二甲基硫醚和危险的强碱,因此该方法几乎不适用于工业生产。该发明提供了一种新化合物1-甲氧基-2,6,10-三甲基-1,3,5,9-十一烯,通过水解和精制该化合物可以制备纯的2-位置双键C-14醛。合成路线简化,非常适合工业生产。
  • Lycopene Intermediate 1, 3, 6, 10-Tetra-Double Bond Pentadec-Carbon Phosphonate as well as Preparation Method and Use Thereof
    申请人:Lao Xuejun
    公开号:US20120330048A1
    公开(公告)日:2012-12-27
    The invention relates to a novel important lycopene intermediate 3,7, 11-trimethyl-1,3,6,10-tetraene-dodecyl diethyl phosphonate. A current lycopene intermediate 2,4,6,10-tetra-double bond pentadec-carbon phosphonate is difficult to synthesize. The invention provides a novel intermediate, which has the following synthesis steps of: preparing 2,6,10-trimethyl-3,5,9-undecane triene-1-aldehyde from pseudoionone; preparing 2,6,10-trimethyl-2,5,9-undecane triene-1-aldehyde from the 2,6,10-trimethyl-3, 5,9-undecane triene-1-aldehyde; and subjecting the 2,6,10-trimethyl-2,5,9-undecane triene-1-aldehyde and tetraethyl methylenediphosphonate to condensation reaction to obtain target product. The invention can generate novel intermediate from raw material pseudoionone only by four reactions, thus the reactions are easy to control and great industrial value are achieved.
    该发明涉及一种新的重要类胡萝卜素中间体3,7,11-三甲基-1,3,6,10-四烯-十二烷基二乙基膦酸酯。目前的类胡萝卜素中间体2,4,6,10-四双键十五碳膦酸酯难以合成。该发明提供了一种新的中间体,其具有以下合成步骤:从伪异香叶酮制备2,6,10-三甲基-3,5,9-十一烯-1-醛;从2,6,10-三甲基-3,5,9-十一烯-1-醛制备2,6,10-三甲基-2,5,9-十一烯-1-醛;并将2,6,10-三甲基-2,5,9-十一烯-1-醛和四乙基甲亚膦酸酯进行缩合反应以获得目标产物。该发明可以仅通过四个反应从原材料伪异香叶酮生成新的中间体,因此反应易于控制且具有重要的工业价值。
  • Method of Preparing 2,6,10-Trimethyl-1,1-Dialkoxy-3,5,9-Undecatriene Used as an Intermediate of Lycopene
    申请人:ZHANG PENGFEI
    公开号:US20120316366A1
    公开(公告)日:2012-12-13
    The present invention describes a novel synthetic method for preparing the key intermediate 2,6,10-trimethyl-1,1-dialkoxy-3,5,9-undecatriene of lycopene. An existing synthetic method have some disadvantages that it is very difficult to gain the raw material dialkyl 4-methyl-5,5-diakoxy-1-pentene-1-phosphonate (10) because no effective synthetic method can be adopted, and furthermore the obtained target compound is composed of several cis/trans isomers. This invention relates to a process comprising a condensation step wherein a starting C10-phosphonate is changed to its carbanion completely at a temperature of −40˜30 under an atmosphere of a non-reactive gas in an organic solvent catalyzed by base, and then C4-dialkyl is added to undergo Wittig-Horner condensation. This invention affords all trans C14-acetal and this method is characterized with the advantages of simple procedure, easy access to raw material and low cost, which makes it has the value of industrial application.
    本发明描述了一种新颖的合成方法,用于制备番茄红素的关键中间体2,6,10-三甲基-1,1-二烷氧基-3,5,9-十一烯。现有的合成方法存在一些缺点,即很难获得原料二烷氧基-4-甲基-5,5-二烷氧基-1-戊烯-1-膦酸酯(10),因为没有有效的合成方法可采用,而且所得目标化合物由几种顄/反异构体组成。本发明涉及一种包括缩合步骤的过程,在该过程中,起始的C10-膦酸酯在非反应性气体氛围下,在有机溶剂中由碱催化完全变为其碳负离子,然后加入C4-二烷基进行威蒂-霍纳缩合。本发明提供了全顄C14-缩醛,该方法具有简单的操作程序、易获得原料和低成本的优点,使其具有工业应用的价值。
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