2-(3-Hydroxy-2-oxopropyl)cyclohexanone | 128135-04-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(3-Hydroxy-2-oxopropyl)cyclohexanone
• 英文别名: 2-(3-Hydroxy-2-oxopropyl)cyclohexan-1-one
• CAS: 128135-04-6
• 化学式: C₉H₁₄O₃
• 分子量: 170.208
• InChiKey: XPQXYLIMCYGBII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(3-Hydroxy-2-oxopropyl)cyclohexanone 在 sodium hydroxide 作用下， 以 甲醇 为溶剂， 反应 1.0h， 以77%的产率得到1-Hydroxy-3,3a,4,5,6,7-hexahydroinden-2-one
  参考文献：
  名称：

  An effective and selective conjugate propargylation reaction of stannylallenes to .alpha.,.beta.-unsaturated carbonyl compounds and .alpha.-nitro olefins

  摘要：

  DOI：

  10.1021/jo00303a019
• 作为产物：
  描述：

  2-(2-propynyl)cyclohexanone 在 silica gel 、 potassium carbonate 、 [双(三氟乙酰氧基)碘]苯 作用下， 生成 2-(3-Hydroxy-2-oxopropyl)cyclohexanone
  参考文献：
  名称：

  An effective and selective conjugate propargylation reaction of stannylallenes to .alpha.,.beta.-unsaturated carbonyl compounds and .alpha.-nitro olefins

  摘要：

  DOI：

  10.1021/jo00303a019

文献信息

• A New and Mild Heterogeneous Catalytic Decomposition of α-Diazo Carbonyl Compounds Using Montmorillonite or Zeolite
  作者：Sengodagounder Muthusamy、Srinivasarao Arulananda Babu、Chidambaram Gunanathan、Raksh Vir Jasra

  DOI：10.1055/s-2002-20452

  日期：——

  A very mild method of decomposition of various α-diazo carbonyl compounds 1 in the presence of environmentally attractive solid acids such as montmorillonite K-10 or zeolite H-Y in a heterogeneous manner to furnish α-hydroxy/alkoxy ketones in very good yield is reported. Interestingly, novel bicycloalkane-1,3-diones and 3-furanones were obtained as unusual products in the case of aliphatic/alicyclic α-diazo carbonyl compounds.

  报告采用一种非常温和的方法，在对环境有吸引力的固体酸（如蒙脱石 K-10 或沸石 H-Y）存在下，以异构方式分解各种δ-重氮羰基化合物 1，从而以非常好的收率得到δ-羟基/烷氧基酮。有趣的是，在脂肪族/脂环族 δ-重氮羰基化合物中，作为不常见的产物，获得了新型双环烷-1,3-二酮和 3-呋喃酮。
• Amberlyst-15 mediated decomposition of α-diazo carbonyl compounds
  作者：Sengodagounder Muthusamy、Srinivasarao Arulananda Babu、Chidambaram Gunanathan、Raksh Vir Jasra

  DOI：10.1016/s0040-4039(01)00936-4

  日期：2001.7

  An efficient heterogeneous catalytic method for the synthesis of alpha -hydroxy ketones from alpha -diazo carbonyl compounds 1, 3 and 6 in the presence of Amberlyst-15. a macro reticular ion exchange resin, is reported. The desired products were obtained at room temperature or by ultrasonication in good yield. Interestingly, novel fused 3-furanones and bicycloalkane-1,3-diones were obtained as unusual products in the case of alicyclic alpha -diazo carbonyl compounds. (C) 2001 Elsevier Science Ltd. All rights reserved.
• HARUTA, JUN-ICHI;NISHI, KOICHI;MATSUDA, SATOSHI;AKAI, SHUJI;TAMURA, YASUM+, J. ORG. CHEM., 55,(1990) N6, C. 4853-4859
  作者：HARUTA, JUN-ICHI、NISHI, KOICHI、MATSUDA, SATOSHI、AKAI, SHUJI、TAMURA, YASUM+

  DOI：——

  日期：——
• An effective and selective conjugate propargylation reaction of stannylallenes to .alpha.,.beta.-unsaturated carbonyl compounds and .alpha.-nitro olefins
  作者：Junichi Haruta、Koichi Nishi、Satoshi Matsuda、Shuji Akai、Yasumitsu Tamura、Yasuyuki Kita

  DOI：10.1021/jo00303a019

  日期：1990.8