(+/-)-2-(4-methylphenyl)-tetrahydro-2H-pyran-4-one | 1026692-59-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (+/-)-2-(4-methylphenyl)-tetrahydro-2H-pyran-4-one
• 英文别名: 2-p-tolyldihydro-2H-pyran-4(3H)-one；2-(4-Methylphenyl)oxan-4-one
• CAS: 1026692-59-0
• 化学式: C₁₂H₁₄O₂
• 分子量: 190.242
• InChiKey: YHEBOYYUEUBYSB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (+/-)-2-(4-methylphenyl)-tetrahydro-2H-pyran-4-one 在 Daucus carota cells 作用下， 以 水 为溶剂， 反应 24.0h， 生成 cis-2-(4-methylphenyl)-4-hydroxy-tetrahydropyran 、 (2S,4S)-2-(4-methylphenyl)-tetrahydro-2H-4-pyranol 、 (2R,4R)-2-(4-methylphenyl)-tetrahydro-2H-4-pyranol 、 (2S,4R)-2-(4-methylphenyl)-tetrahydro-2H-4-pyranol
  参考文献：
  名称：

  Enantioselective reduction of 2-substituted tetrahydropyran-4-ones using Daucus carota plant cells

  摘要：

  Enzymatic reduction of 2-substituted tetrahydropyran-4-ones with Daucus carota, plant cells as biocatalyst occurred in water under extremely mild and environmentally benign conditions giving a 1:1 mixture of diastereoselectively (2R,4S)- and (2S,4S)-2-aryl- or 2-alkyl-tetrahydropyranois in high yields. (c) 2008 Published by Elsevier Ltd.

  DOI：

  10.1016/j.tetlet.2008.02.131
• 作为产物：
  描述：

  4-(4-methylbenzyloxy)but-1-en-2-yl acetate 在 2,6-二氯吡啶 、 manganese(IV) oxide 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 硝基甲烷 为溶剂， 反应 44.25h， 以83%的产率得到(+/-)-2-(4-methylphenyl)-tetrahydro-2H-pyran-4-one
  参考文献：
  名称：

  2,3-Dichloro-5,6-dicyano-1,4-benzoquinone-Catalyzed Reactions Employing MnO₂ as a Stoichiometric Oxidant

  摘要：

  Several oxidative reactions can be effected with MnO2 in the presence of substoichiometric quantities of DDQ. These transformations include oxidative cyclization, deprotection, and dehydrogenation reactions. The use of MnO2 as a terminal oxidant for DDQ-mediated reactions is attractive based on economical and environmental factors.

  DOI：

  10.1021/ol102078v

文献信息

• Mechanistic analysis of oxidative C–H cleavages using inter- and intramolecular kinetic isotope effects
  作者：Hyung Hoon Jung、Paul E. Floreancig

  DOI：10.1016/j.tet.2009.10.088

  日期：2009.12

  series of monodeuterated benzylic and allylic ethers were subjected to oxidative carbon–hydrogen bond cleavage to determine the impact of structural variation on intramolecular kinetic isotope effects in DDQ-mediated cyclization reactions. These values are compared to the corresponding intermolecular kinetic isotope effects that were accessed through subjecting mixtures of non-deuterated and dideuterated

  对一系列单氘代苄基醚和烯丙基醚进行氧化碳氢键断裂，以确定结构变化对 DDQ 介导的环化反应中分子内动力学同位素效应的影响。将这些值与通过将非氘化和双氘化底物的混合物置于反应条件下获得的相应分子间动力学同位素效应进行比较。结果表明，碳氢键断裂是速率决定因素，自由基阳离子很可能是反应机制中的关键中间体。
• A novel self-terminated Prins strategy for the synthesis of tetrahydropyran-4-one derivatives and their behaviour in Fisher indole synthesis
  作者：B. V. Subba Reddy、S. Rehana Anjum、B. Sridhar

  DOI：10.1039/c6ra11218h

  日期：——

  has been developed for the synthesis of 2-substituted tetrahydropyran-4-one derivatives through a condensation of 3-(phenylthio)but-3-en-1-ol with carbonyl compounds in the presence of 5 mol% of Sc(OTf)3 under mild conditions. A few products were subsequently transformed into the corresponding indoles by Fisher-indole synthesis.

  已开发出一种新颖的自封端Prins策略，用于在5 mol存在下通过3-（苯硫基）but-3-en-1-醇与羰基化合物的缩合反应合成2-取代的四氢吡喃-4-酮衍生物。在温和条件下的Sc（OTf）3的百分比。随后通过费希尔-吲哚合成将一些产物转化为相应的吲哚。
• 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone-Catalyzed Reactions Employing MnO₂ as a Stoichiometric Oxidant
  作者：Lei Liu、Paul E. Floreancig

  DOI：10.1021/ol102078v

  日期：2010.10.15

  Several oxidative reactions can be effected with MnO2 in the presence of substoichiometric quantities of DDQ. These transformations include oxidative cyclization, deprotection, and dehydrogenation reactions. The use of MnO2 as a terminal oxidant for DDQ-mediated reactions is attractive based on economical and environmental factors.
• Enantioselective reduction of 2-substituted tetrahydropyran-4-ones using Daucus carota plant cells
  作者：J.S. Yadav、B.V. Subba Reddy、Ch. Sreelakshmi、G.G.K.S. Narayana Kumar、A. Bhaskar Rao

  DOI：10.1016/j.tetlet.2008.02.131

  日期：2008.4

  Enzymatic reduction of 2-substituted tetrahydropyran-4-ones with Daucus carota, plant cells as biocatalyst occurred in water under extremely mild and environmentally benign conditions giving a 1:1 mixture of diastereoselectively (2R,4S)- and (2S,4S)-2-aryl- or 2-alkyl-tetrahydropyranois in high yields. (c) 2008 Published by Elsevier Ltd.