3-丁基-2-苯基环戊-2-烯-1-酮 | 96405-96-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-丁基-2-苯基环戊-2-烯-1-酮
• 英文名称: 3-butyl-2-phenyl-2-cyclopenten-1-one
• 英文别名: 3-Butyl-2-phenyl-2-cyclopenten-1-on；2-phenyl-3-butylclopenten-1-one；3-Butyl-2-phenylcyclopent-2-en-1-one
• CAS: 96405-96-8
• 化学式: C₁₅H₁₈O
• 分子量: 214.307
• InChiKey: OKQIKMWUKNTDIE-UHFFFAOYSA-N

物化性质

• 沸点：
  102-103 °C(Press: 0.01 Torr)
• 密度：
  1.024±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  苯丙酮酸 在 3-苄基羟乙基甲基噻唑氯化锂 sodium hydroxide 、 三乙胺 作用下， 以 乙醇 为溶剂， 反应 6.0h， 生成 3-丁基-2-苯基环戊-2-烯-1-酮
  参考文献：
  名称：

  Stetter, Hermann; Lorenz, Guenther, Chemische Berichte, 1985, vol. 118, # 3, p. 1115 - 1125

  摘要：

  DOI：

文献信息

• Preparation and reactions of monocyclic bis(cyclopentadienyl)titanacyclopentenes and -pentadienes
  作者：Kimihiko Sato、Yasushi Nishihara、Shouquan Huo、Zhenfeng Xi、Tamotsu Takahashi

  DOI：10.1016/s0022-328x(01)01072-5

  日期：2001.8

  be very effective for the formation of monocyclic titanacyclopentenes in excellent yields. On the other hand, a combination of Cp2TiCl2–2n-BuLi was used for intermolecular coupling of two alkynes to form titanacyclopentadienes in good to excellent yields. A reaction temperature range from −10 to −30 °C was critical for the success of the combinations. Reactions of these in situ-prepared titanacycles

  发现Cp 2 TiCl 2 –2EtMgBr的组合对于形成单环钛环戊烯非常有效，并且产率很高。另一方面，将Cp 2 TiCl 2 –2 n -BuLi的组合用于两个炔烃的分子间偶联，形成钛环戊二烯，收率好至极好。-10至-30°C的反应温度范围对于组合的成功至关重要。这些原位制备的钛环化合物的反应显示出与它们的氧化锆环类似物有趣或相似的区别。
• Oxidative Conversion of Silyl Enol Ethers to α,β-Unsaturated Ketones Employing Oxoammonium Salts
  作者：Masaki Hayashi、Masatoshi Shibuya、Yoshiharu Iwabuchi

  DOI：10.1021/ol2029417

  日期：2012.1.6

  The oxidative conversion of silyl enol ethers to α,β-unsaturated ketones using a less-hindered class of oxoammonium salts (AZADO+BF4–) is described. The reaction proceeds via the ene-like addition of oxoammonium salts to silyl enol ethers.

  描述了使用较少受阻的一类氧铵盐（AZADO + BF 4 –）将甲硅烷基烯醇醚氧化转化为α，β-不饱和酮的方法。该反应通过类似烯的氧代铵盐加成到甲硅烷基烯醇醚中而进行。
• Catalytic Intermolecular Pauson−Khand-Type Reaction:  Strong Directing Effect of Pyridylsilyl and Pyrimidylsilyl Groups and Isolation of Ru Complexes Relevant to Catalytic Reaction
  作者：Kenichiro Itami、Koichi Mitsudo、Kazuyoshi Fujita、Youichi Ohashi、Jun-ichi Yoshida

  DOI：10.1021/ja047484+

  日期：2004.9.1

  Some circumstantial evidence for the directing effect of the 2-pyridylsilyl group in the Ru-catalyzed intermolecular Pauson-Khand-type reaction (PKR) of alkenyl(2-pyridyl)silane, alkyne, and carbon monoxide has been provided. Most importantly, we have succeeded in isolating several monometallic Ru complexes relevant to the catalytic reaction: Ru(vinylsilane)(CO)(3) complexes and ruthenacyclopentene. While the stoichimetric reaction of the Ru(vinylsilane)(CO)(3) complex with an alkyne led to the formation of the corresponding cyclopentenone (PKR product) at 100 degreesC, the ruthenacyclopentene intermediate was quantitatively produced at 50 degreesC. This complex was also converted to a cyclopentenone upon heating at 100 degreesC. Moreover, it was also found that the Ru(vinylsilane)(CO)(3) complex and ruthenacyclopentene serve as catalysts in intermolecular PKR.
• STETTER, H.;LORENZ, G., CHEM. BER., 1985, 118, N 3, 1115-1125
  作者：STETTER, H.、LORENZ, G.

  DOI：——

  日期：——
• Stetter, Hermann; Lorenz, Guenther, Chemische Berichte, 1985, vol. 118, # 3, p. 1115 - 1125
  作者：Stetter, Hermann、Lorenz, Guenther

  DOI：——

  日期：——