(E)-4-(2'-propenyl)-1,5-heptadien-4-ol | 101536-77-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (E)-4-(2'-propenyl)-1,5-heptadien-4-ol
• 英文别名: diallyl-(1-propenyl)carbinol；4-allyl-hepta-1,5t-dien-4-ol；(5E)-4-prop-2-enylhepta-1,5-dien-4-ol
• CAS: 101536-77-0
• 化学式: C₁₀H₁₆O
• 分子量: 152.236
• InChiKey: IRPAPFUYRIBKJO-RMKNXTFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  11
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.4
• 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：

  (E)-4-(2'-propenyl)-1,5-heptadien-4-ol 生成 6-methyl-1,8-nonadien-4-one
  参考文献：
  名称：

  SNOWDEN, ROGER L.;LINDER, SIMON M.;MULLER, BERNARD L.;SCHULTE-ELTE, KARL +, HELV. CHIM. ACTA, 70,(1987) N 7, 1858-1878

  摘要：

  DOI：
• 作为产物：
  描述：

  4-(2-氯-丙基)-庚-1,6-二烯-4-醇 在 正丁基锂 作用下， 生成 (E)-4-(2'-propenyl)-1,5-heptadien-4-ol
  参考文献：
  名称：

  γ-Substituted Secondary Organoalkaline Compounds and their Chlorinated Precursors: Synthetic Applications

  摘要：

  本文描述了从甲基3-氯丁酸酯（通过氢氯酸与市售的甲基反式-2-丁烯酸酯的加成获得）出发，制备γ-功能化二级有机碱金属化合物的方法。这些金属化合物的反应与适当的亲电试剂结合，可以生成多种三级醇衍生物。

  DOI：

  10.1055/s-1985-31362

文献信息

• ?-Cleavage of Bis(homoallylic) Potassium Alkoxides. Two-Step Preparation of Propenyl Ketones from Carboxylic Esters. Synthesis ofar-Turmerone, ?-Damascone, ?-Damascone, and ?-Damascenone
  作者：Roger L. Snowden、Simon M. Linder、Bernard L. Muller、Karl H. Schulte-Elte

  DOI：10.1002/hlca.19870700721

  日期：1987.11.4

  The transformation of 36 bis(homoallylic) alcohols VII to alkenones IX and Xvia β-cleavage of their potassium alkoxides VIIa in HMPA has been investigated (cf. Scheme 2). These studies have established an order of β-cleavage for 2-propenyl, 1-methyl-2propenyl, 2-methyl-2-propenyl, 1,1-dimethyl-2propenyl, and benzyl groups in alkoxides 49a–56a and have allowed a comparison between the β-cleavege reaction

  已经研究了在HMPA中通过36个双（均烯丙基）醇VII的醇钾VIIa的β裂解转化为烯酮IX和X的方法（参见方案2）。这些研究建立了醇盐49a – 56a中2-丙烯基，1-甲基-2丙烯基，2-甲基-2-丙烯基，1,1-二甲基-2丙烯基和苄基的β裂解顺序，并允许进行比较β裂解反应与烷氧化物74a – 83a中的氧化Cope重排之间的关系。作为示例性的合成应用，丙烯醛的两步制备15 –42从羧酸酯中描述，用合成在一起AR -turmerone（48），α二氢大马酮（（ë） - 71），β大马酮（（ë） - 109），和β大马酮（（ë） - 111）。
• Metal zinc-promoted gem -bisallylation of acid chlorides with allyl chlorides in the presence of chlorotrimethylsilane
  作者：Yoshio Ishino、Masatoshi Mihara、Manabu Kageyama

  DOI：10.1016/s0040-4039(02)01437-5

  日期：2002.9

  Treatment of acid chlorides (2) with allyl chlorides (1) in the presence of zinc dust and a catalytic amount of chlorotrimethylsilane (TMSCl) in THF brought about highly facile and effective coupling to give the corresponding gem-bisallylation products. 4-hydroxy-penta-1,6-dienes (3), in good to excellent yields. These reactions are assumed to proceed through allylzinc intermediates generated in situ. (C) 2002 Elsevier Science Ltd. All rights reserved.
• An efficient of Grignard-type procedure for the preparation of gem-diallylated compound
  作者：Kao-Hsien Shen、Chun-Wei Kuo、Ching-Fa Yao

  DOI：10.1016/j.tetlet.2007.07.008

  日期：2007.9

  An efficient and a new procedure for the conversion of various carboxylic acid derivatives into the corresponding gemdiallylated compound under mild reaction condition has been developed. The triallyaluminum mediated Grignard-type addition of carboxylic acid derivative was utilized as a key operation to affect the transformation. The procedure is operationally simple, giving good to excellent product yields for a broad range of substrates. The chemoselectivity and regioselectivity of triallylaluminum were also demonstrated. (C) 2007 Elsevier Ltd. All rights reserved.
• ?-Complexes of transition metals in organic synthesis 8. Coupled addition of allyl MN(II)-organic compounds to esters and nitriles of?,?-unsaturated carboxylic acids
  作者：A. N. Kasatkin、O. Yu. Tsypyshev、T. Yu. Romanova、G. A. Tolstikov

  DOI：10.1007/bf00961710

  日期：1990.5

  Allyl Mn(II)-organic compounds R1CH = C(R2).CH2MnCl (R1 = H, Me; R2 = H, Me, Bu, PhCH2) react with esters and nitriles of crotonic, trans-2-hexenoic, sorbic, cinnamic, maleic, fumaric, heptylidenemalonic, and trans-(2-butenylidene)malonic acids in THF at -78 to -60-degrees-C giving 1,4-addition products. A single diastereoisomer is formed in the case of MeCH = CHCO2Me and PrCH = CHCO2Me.
• Munch-Petersen et al., Acta Chemica Scandinavica (1947), 1959, vol. 13, p. 1955,1957
  作者：Munch-Petersen et al.

  DOI：——

  日期：——