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(5R,7R)-7-Methyl-1,6-dioxaspiro<4.5>decane | 209248-22-6

中文名称
——
中文别名
——
英文名称
(5R,7R)-7-Methyl-1,6-dioxaspiro<4.5>decane
英文别名
(E)-(5R,7R)-(+)-7-Methyl-1,6-dioxaspiro[4.5]decane;(5R,7R)-(+)-7-methyl-1,6-dioxaspiro[4.5]decane;(5R,7R)-7-Methyl-1,6-dioxaspiro[4.5]decane
(5R,7R)-7-Methyl-1,6-dioxaspiro<4.5>decane化学式
CAS
209248-22-6
化学式
C9H16O2
mdl
——
分子量
156.225
InChiKey
XNNASGSBOJGKAZ-RKDXNWHRSA-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

物化性质

  • 沸点:
    201.7±8.0 °C(Predicted)
  • 密度:
    1.01±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    1-(tetrahydropyran-2-yloxy)non-8-en-4-one 在 W-Raney-Ni camphor-10-sulfonic acid 、 氢气 、 zinc dibromide 作用下, 以 甲醇乙醚二氯甲烷 为溶剂, 反应 7.5h, 生成 (5R,7R)-7-Methyl-1,6-dioxaspiro<4.5>decane
    参考文献:
    名称:
    Doherty, Annette M.; Ley, Steven V.; Lygo, Barry, Journal of the Chemical Society. Perkin transactions I, 1984, p. 1371 - 1378
    摘要:
    DOI:
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文献信息

  • Synthesis of Spiroacetal Pheromones via Metalated Hydrazones
    作者:Dieter Enders、Walter Dahmen、Eleonore Dederichs、Winfried Gatzweiler、Peter Weuster
    DOI:10.1055/s-1990-27080
    日期:——
    The synthesis of simple alkyl substituted spiroacetals by α,α′-alkylation of metalated acetone dimethylhydrazone with appropriate electrophiles and subsequent acid catalyzed cleavage and ring closure of the products is described.
    通过合适的亲电试剂与金属化丙酮二甲基脲的α,α′-烷基化反应,随后进行酸催化的断裂和环化闭合,描述了简单烷基取代螺缩醛的合成方法。
  • Wittig and horner-wittig coupling reactions of 2-substituted cyclic ethers and their application to spiroketal synthesis
    作者:Steven V Ley、Barry Lygo、Helen M. Organ、Anne Wonnacott
    DOI:10.1016/s0040-4020(01)91403-6
    日期:1985.1
    Wittig and Horner-Wittig coupling reactions of tetrahydropyran or tetrahydrofuran 2-triphenylphosphonium salts or 2-diphenylphosphine oxides with aldehydes and lactols affords good yields of the corresponding enol ethers. In selected examples these enol ether products may be further converted to spiroketals some of which are natural pheromones derived from Dacus oleae and Paravespula vulgaris.
    四氢吡喃或四氢呋喃2-三苯基phosph盐或2-二苯基膦氧化物与醛和乳糖醇的Wittig和Horner-Wittig偶联反应提供了良好的相应烯醇醚产率。在选定的实例中,这些烯醇醚产物可以进一步转化为螺环酮,其中一些是得自油茶和寻常型草的天然信息素。
  • Synthesis of optically active 2s-, and 7s-methyl-1.6-dioxa-spiro[4.5] decane, the pheromone components of Paravespula vulgaris (L.), from S-ethyl lactate.
    作者:K. Hintzer、R. Weber、V. Schurig
    DOI:10.1016/0040-4039(81)80039-1
    日期:1981.1
    (−)-2S, 5RS-1 and (−]-7S, 5S-2 are obtained from S-ethyl lactate 4 and their absolute configuration is thus directly correlated. Accurate enantiomeric compositions of intermediates and products were measured by complexation gas chromatography on nickel-, and manganese-bis-3-heptafluorobutyryl-1R-camphorate, 3. It could be conclusively established that the syntheses proceed with a high degree of preservation
    (-)-2S,5RS-1和(-]-7S,5S-2是由乳酸S-乙酯4得到的,因此它们的绝对构型直接相关,中间体和产物的精确对映体组成通过络合气相色谱法测定。镍-和锰-双-3-3七氟丁酰-1R-樟脑膦酸酯3.可以确定地确定合成过程在高度保留构型的情况下进行。
  • Syntheses photochimiques de dioxa-1,6 spiro[4.5] decanes pheromones de paravespula vulgaris L
    作者:Tomasz Koźluk、Louis Cottier、Gérard Descotes
    DOI:10.1016/s0040-4020(01)97936-0
    日期:——
    A general approach to 1-6 dioxa[4.5]spirodecanes is presented and applied to the total synthesis of one pheromone of Paravespula vulgaris L.
    提出了一种一般的方法,对1-6个二恶英[4.5]螺旋十二烷进行了研究,并将其应用于杂草副生菜的一种信息素的全合成。
  • Spiroacetals and Other Venom Constituents as Potential Wasp Attractants
    作者:Roderick J. Weston、Anthony D. Woolhouse、Eric B. Spurr、Richard J. Harris、D. Max Suckling
    DOI:10.1023/b:joec.0000006396.55680.b6
    日期:1997.3
    The major volatile spiroacetals from the venom of both the common wasp, Vespula vulgaris and the German wasp V. germanica, viz. 7-methyl-1,6-dioxaspiro[4,5]decane and 7-ethyl-2-methyl-1,6-dioxaspiro[4,5]decane, respectively, were synthesized by known methods. These acetals, along with N-isopentylacetamide (the major volatile amide from wasp venom), 2-heptanone (a honeybee pheromone), 2-methyl-3-buten-2-ol (a component of hornet venom), cuticle wax from V. vulgaris, and venom sacs from both wasp species were assayed by EAG and olfactory bioassay for attractancy to V. vulgaris workers. Antennal responses to all test chemicals were recorded. Acetal isomers (+/-)-2 and (+/-)-3, N-isopentylacetamide, and 2-heptanone were attractive to V. vulgaris workers at levels of <1 mu mol. Greater quantities of the same compounds were repellent to V. vulgaris workers.
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