十一碳-5-炔酸 | 822-02-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 中文名称: 十一碳-5-炔酸
• 英文名称: 5-undecynoic acid
• 英文别名: Undec-5-insaeure；5-Undecinsaeure；undec-5-ynoic acid
• CAS: 822-02-6
• 化学式: C₁₁H₁₈O₂
• 分子量: 182.263
• InChiKey: UFVXTAPZDFGWBH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  13
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  十一碳-5-炔酸 在 Lindlar's catalyst 氢气 作用下， 以91%的产率得到(Z)-5-undecenoic acid
  参考文献：
  名称：

  Huhtasaari, Matti; Schaefer, Hans J.; Luftmann, Heinrich, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1983, vol. 37, # 6, p. 537 - 548

  摘要：

  DOI：
• 作为产物：
  描述：

  1-cyano-4-decyne 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 96.0h， 以78%的产率得到十一碳-5-炔酸
  参考文献：
  名称：

  Huhtasaari, Matti; Schaefer, Hans J.; Luftmann, Heinrich, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1983, vol. 37, # 6, p. 537 - 548

  摘要：

  DOI：

文献信息

• Dianion of Sulfinylacetone as a Synthetic Equivalent of .BETA.-Enolate of Propionic Acid: A Novel Synthesis of Carboxylic Acids from Alkyl Halides with Three-Carbon Elongation
  作者：Tsuyoshi Satoh、Kentaro Imai

  DOI：10.1248/cpb.51.602

  日期：——

  dianion of phenylsulfinylacetone with alkyl halides afforded beta-keto sulfoxides, which were first chlorinated with hexachloroethane and then treated successively with KH and t-BuLi to give carboxylic acids in three-steps in moderate overall yields from the alkyl halides. This procedure affords a good method for a synthesis of carboxylic acids from alkyl halides with three-carbon elongation.

  苯亚磺酰基丙酮的二价阴离子与卤代烷反应生成的β-酮亚砜，先用六氯乙烷进行氯化处理，然后依次用KH和t-BuLi处理，分三步从卤代烷中以总产率适中的方式得到羧酸。该程序为由具有三碳延伸率的卤代烷合成羧酸提供了一种很好的方法。
• Suppression of β-Hydride Elimination in the Intramolecular Hydrocarboxylation of Alkynes leading to the Formation of Lactones
  作者：Zhibao Huo、Nitin T. Patil、Tienan Jin、Nirmal K. Pahadi、Yoshinori Yamamoto

  DOI：10.1002/adsc.200600507

  日期：2007.3.5

  Palladium-catalyzed intramolecular cyclization of the alkynoic acids was studied which gave the five- and six-membered lactones in moderate yields. The reaction can be conducted simply by heating a toluene solution of alkynoic acids at 100 °C in the presence of catalytic amounts of Pd(PPh3)4 and (o-tol)3P. The key for this transformation is the use of phosphines, instead of carboxylic acids, as an

  研究了钯催化的炔酸分子内环化反应，得到中等价位的五元和六元内酯。该反应可以简单地通过在催化量的Pd（PPh 3）4和（o- tol）3 P存在下于100°C加热炔酸的甲苯溶液进行。该转化的关键是使用膦代替羧酸作为添加剂。与我们先前开发的催化体系相似，使用羧酸代替（邻甲苯基）3 P导致了二烯的排他性形成。
• Palladium-catalyzed intramolecular addition of amines to acetylenes. Synthesis of cyclic imines
  作者：Yukitoshi Fukuda、Seijiro Matsubara、Kiitiro Utimoto

  DOI：10.1021/jo00020a023

  日期：1991.9

  Intramolecular aminopalladation of alkynylamines gave intermediary alkenylpalladium compounds that hydrolyzed and isomerized to thermodynamically stable cyclic imines. Treatment of 3-alkynylamines with a catalytic amount of PdCl2(MeCN)2 gave exclusively 1-pyrrolines in good yields; 5-alkynylamines afforded 2,3,4,5-tetrahydropyridines selectively. Treatment of 4-alkynylamines with Pd(II) afforded mixtures of both 5- and 6-membered cyclic imines. Applications to the synthesis of some naturally occurring alkaloids are also described.
• 164. Syntheses of long-chain acids. Part VI. Acetylenic acids and cis,cis-docosa-5,13-dienoic acid
  作者：D. E. Ames、A. N. Covell、T. G. Goodburn

  DOI：10.1039/jr9650000894

  日期：——
• New functions of (arene)tricarbonylchromium(0) complexes as hydrogenation catalysts: stereospecific semihydrogenation of alkynes and highly chemoselective hydrogenation of .alpha.,.beta.-unsaturated carbonyl compounds
  作者：Mikiko Sodeoka、Masakatsu Shibasaki

  DOI：10.1021/jo00207a056

  日期：1985.4