3-(3-cyclohexenyl)propanoic acid | 76837-82-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 3-(3-cyclohexenyl)propanoic acid
• 英文别名: 3-(3-Cyclohexenyl)propionic acid；3--propionsaeure；(+/-)-3--propionsaeure；(+/-)-3-(cyclohex-2-enyl)propanoic acid；3-(2-Cyclohexen-1-yl)propanoic acid；3-cyclohex-2-en-1-ylpropanoic acid
• CAS: 76837-82-6
• 化学式: C₉H₁₄O₂
• 分子量: 154.209
• InChiKey: MNGWBZXJEJOWMJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  11
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 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：

  3-(3-cyclohexenyl)propanoic acid 在 氯磷酸二乙酯 、 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 16.0h， 生成 Se-phenyl 3-(3-cyclohexenyl)propaneselenoate
  参考文献：
  名称：

  Acyl radicals: intermolecular and intramolecular alkene addition reactions

  摘要：

  A full study of the use of phenyl selenoesters as precursors to acyl radicals and their subsequent participation in intermolecular and intramolecular alkene addition reactions is detailed. Primary alkyl-, vinyl-, and aryl-substituted acyl radicals generated by Bu3SnH treatment of the corresponding phenyl selenoesters participate cleanly in intermolecular addition reactions with alkenes bearing electron-withdrawing or radical-stabilizing substituents at rates that exceed those of the potentially competitive decarbonylation or reduction. Similarly, their intramolecular addition to activated or unactivated alkenes proceeds without significant competitive reduction or decarbonylation and at rates generally greater-than-or-equal-to 1 x 10(6) s-1 with some occurring at rates greater-than-or-equal-to 3 x 10(7) s-1. Consistent with their behavior in intermolecular addition reactions, the 5-exo-trig cyclizations of secondary and tertiary alkyl-substituted acyl radicals to an unactivated olefin acceptor may be accompanied by varying degrees of decarbonylation, even under low-temperature free-radical reaction conditions. Studies are presented which suggest that the intramolecular additions of acyl radicals to alkenes under the conditions detailed herein may be regarded as irreversible, kinetically controlled processes which exhibit regioselectivity that is predictable based on well-established empirical rules set forth for the analogous free-radical cyclization reactions of alkyl radicals.

  DOI：

  10.1021/jo00031a021
• 作为产物：
  描述：

  2-(cyclohex-2-enyl)ethanol 在 苄基三乙基氯化铵 sodium hydroxide 作用下， 以 吡啶 、 水 、 二甲基亚砜 为溶剂， 反应 29.0h， 生成 3-(3-cyclohexenyl)propanoic acid
  参考文献：
  名称：

  Turecek, Frantisek, Collection of Czechoslovak Chemical Communications, 1982, vol. 47, # 3, p. 858 - 876

  摘要：

  DOI：

文献信息

• Stereocontrolled Synthesis of Substituted Bicyclic Ethers through Oxy-Favorskii Rearrangement: Total Synthesis of (±)-Communiol E
  作者：Shoji Kobayashi、Tatsuhiro Kinoshita、Takuji Kawamoto、Masato Wada、Hiroyuki Kuroda、Araki Masuyama、Ilhyong Ryu

  DOI：10.1021/jo201064h

  日期：2011.9.2

  The potential of the oxy-Favorskii rearrangement to form branched cis-fused bicyclic ethers was explored. Both tertiary and quaternary centers were constructed in highly stereospecific manners. Methanol and primary amines were effective nucleophiles for the rearrangement. The total synthesis of (±)-communiol E was achieved based on this method.

  探索了氧基-Favorskii重排形成支链顺式稠合双环醚的潜力。三级和四级中心都是以高度立体化的方式构建的。甲醇和伯胺是有效的重排亲核试剂。基于该方法，实现了（±）-香酚E的全合成。
• Lithiated cyclopropanone ketals
  作者：Paul Dowd、Christopher Kaufman、Paul Kaufnan、Yi Hyon Paik

  DOI：10.1016/s0040-4039(00)95074-3

  日期：1985.1

  The ketene acetal I reacted with dibromocarbene yielding the dibromocyclopropanone ketal II, which was reduced to the monobromide III by treatment with tri-n-butyltin hydride. Reaction of III with n-butyllithium at −78°C yielded the lithiated cyclopropanone ketal IV, which yielded adducts with acetone, cyclohexanone, cyclohexenone, 3,3,3-trimethoxybutan-2-one, 2-butanone, and 3-pentanone.

  乙烯酮缩醛Ⅰ与二溴卡宾反应生成二溴环丙烷酮缩酮Ⅱ，通过用氢化三正丁基锡处理将其还原为一溴化物Ⅲ。III在-78°C下与正丁基锂反应生成锂化的环丙烷酮缩酮IV，从而生成与丙酮，环己酮，环己烯酮，3,3,3-三甲氧基丁-2--2-，2-丁酮和3-戊酮的加合物。
• Heat transfer fluid corrosion inhibitors
  申请人：TEXACO DEVELOPMENT CORPORATION

  公开号：EP0573287A1

  公开（公告）日：1993-12-08

  Corrosion inhibitors containing alkanoic, hydrocarbyl dicarboxylic and carbocyclic-substituted, alkanoic acids or salts give high performance, heat transfer fluids and antifreezes, with improved properties including storage stability.

  含有烷酸、烃基二羧酸和碳环取代的烷酸或盐的缓蚀剂可提供高性能的传热流体和防冻剂，并具有更好的性能，包括储存稳定性。
• Julia,M. et al., Bulletin de la Societe Chimique de France, 1964, p. 1116 - 1122
  作者：Julia,M. et al.

  DOI：——

  日期：——
• Claisen rearrangements of lactonic (silyl) enolates: a new route to functionalized cycloalkenes
  作者：Samuel Danishefsky、Raymond L. Funk、James F. Kerwin

  DOI：10.1021/ja00542a058

  日期：1980.10