3-(4-acetylphenyl)cyclopent-2-en-1-one | 1107640-94-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-(4-acetylphenyl)cyclopent-2-en-1-one
• 英文别名: 3-(4-Acetylphenyl)cyclopent-2-en-1-one
• CAS: 1107640-94-7
• 化学式: C₁₃H₁₂O₂
• 分子量: 200.237
• InChiKey: OMWHNQQYRYXNFQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-(4-acetylphenyl)cyclopent-2-en-1-one 在 bis(norbornadiene)rhodium(l)tetrafluoroborate 、 ferrocene 、 氢气 作用下， 以 甲苯 为溶剂， 35.0 ℃ 、3.04 MPa 条件下， 以99%的产率得到(R)-3-(4-acetylphenyl)cyclopentan-1-one
  参考文献：
  名称：

  内环烯酮的对映选择性加氢：历史问题的解决方案†

  摘要：

  内环烯酮的对映选择性氢化一直是均相催化的历史问题。我们在本文中报道了一种用分子氢还原内环烯酮的有效方法。在铑/ Zhaophos配合物的催化下，具有五，六或七元环的各种烯酮以高对映选择性（92％-99％ee）氢化。出色的化学和对映选择性证明了该方法已成功地用于柠檬醛的对映选择性加氢，以生产对映体富集的香茅醛。

  DOI：

  10.1002/cjoc.202000617
• 作为产物：
  描述：

  2-环戊烯酮 、 4-溴苯乙酮 在 potassium fluoride 、 palladium diacetate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以62%的产率得到3-(4-acetylphenyl)cyclopent-2-en-1-one
  参考文献：
  名称：

  Selective Heck reaction of aryl bromides with cyclopent-2-en-1-one or cyclohex-2-en-1-one

  摘要：

  The selective Heck reaction of cyclopent-2-en-1-one or cyclohex-2-en-1-one with aryl bromides gives a simple access to the corresponding 3-arylcycloalk-2-en-1-ones. The choice of the base was found to be crucial to avoid the formation of 3-arylcyclopentanones or 3-arylcyclohexanones as side-products. Using KF as base, DMF as solvent and Pd(OAc)(2) as catalyst, the target products were obtained in moderate to good yields with a variety of aryl bromides. Substituents such as fluoro, trifluoromethyl, acetyl, benzoyl, formyl, ester or nitrile on the aryl bromide are tolerated. Sterically congested aryl bromides or bromopyridines can also be employed. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2008.11.006

文献信息

• CALCIUM-SENSING RECEPTOR-ACTIVE COMPOUNDS
  申请人：Mansson Kristoffer

  公开号：US20130245084A1

  公开（公告）日：2013-09-19

  Compounds of general formula (I) their use as calcium receptor-active compounds for the prophylaxis, treatment or amelioration of physiological disorders or diseases associated with disturbances of CaSR activity, such as hyperparathyroidism, pharmaceutical compositions comprising said compounds, and methods of treating diseases with said compounds.

  通式（I）的化合物，其用作钙受体活性化合物，用于预防、治疗或改善与CaSR活性紊乱相关的生理障碍或疾病，如甲状旁腺功能亢进症，包括该化合物的制药组合物以及使用该化合物治疗疾病的方法。
• Selective Heck reaction of aryl bromides with cyclopent-2-en-1-one or cyclohex-2-en-1-one
  作者：Yacoub Fall、Henri Doucet、Maurice Santelli

  DOI：10.1016/j.tet.2008.11.006

  日期：2009.1

  The selective Heck reaction of cyclopent-2-en-1-one or cyclohex-2-en-1-one with aryl bromides gives a simple access to the corresponding 3-arylcycloalk-2-en-1-ones. The choice of the base was found to be crucial to avoid the formation of 3-arylcyclopentanones or 3-arylcyclohexanones as side-products. Using KF as base, DMF as solvent and Pd(OAc)(2) as catalyst, the target products were obtained in moderate to good yields with a variety of aryl bromides. Substituents such as fluoro, trifluoromethyl, acetyl, benzoyl, formyl, ester or nitrile on the aryl bromide are tolerated. Sterically congested aryl bromides or bromopyridines can also be employed. (C) 2008 Elsevier Ltd. All rights reserved.
• Enantioselective Hydrogenation of Endocyclic Enones: the Solution to a Historical Problem ^†
  作者：Qiwei Lang、Huaxin Yang、Guoxian Gu、Qiang Feng、Jialin Wen、Xumu Zhang

  DOI：10.1002/cjoc.202000617

  日期：2021.4

  The enantioselective hydrogenation of endocyclic enones has been a historical problem for homogeneous catalysis. We herein report an efficient method to reduce endocyclic enones with molecular hydrogen. Catalyzed by a rhodium/Zhaophos complex, a variety of enones with five‐, six‐ or seven‐member ring were hydrogenated with high enantioselectivity (92%—99% ee). Excellent chemo‐ and enantioselectivity

  内环烯酮的对映选择性氢化一直是均相催化的历史问题。我们在本文中报道了一种用分子氢还原内环烯酮的有效方法。在铑/ Zhaophos配合物的催化下，具有五，六或七元环的各种烯酮以高对映选择性（92％-99％ee）氢化。出色的化学和对映选择性证明了该方法已成功地用于柠檬醛的对映选择性加氢，以生产对映体富集的香茅醛。