6-chloro-4,4-dimethylcyclohex-2-en-1-one | 63577-30-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-chloro-4,4-dimethylcyclohex-2-en-1-one
• 英文别名: 6-Chlor-4,4-dimethyl-2-cyclohexenon
• CAS: 63577-30-0
• 化学式: C₈H₁₁ClO
• 分子量: 158.628
• InChiKey: AHTDWNUURYZPAS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  6-chloro-4,4-dimethylcyclohex-2-en-1-one 在 lithium dimethylcuprate 作用下， 以 乙醚 为溶剂， 反应 0.5h， 以53%的产率得到6-(6-chloro-4,4-dimethyl-1-hydroxycyclohex-2-enyl)-4,4-dimethylcyclohex-2-en-1-one
  参考文献：
  名称：

  Functional group hybrids. Reactivity of .alpha.'-nucleofuge .alpha.,.beta.-unsaturated ketones. 1. Reactions with organocopper reagents

  摘要：

  A series of alpha-nucleofuge alpha',beta'-unsaturated ketones encompassing a variety of structural types and nucleofuges was prepared. Treatment of these compounds with lithium dimethylcuprate or methylcopper leads primarily to either reductive cleavage of the alpha-nucleofuge or conjugate addition. Good alpha-nucleofuges favored the reduction pathway while poorer nucleofuges favored conjugate addition.

  DOI：

  10.1021/jo00024a014
• 作为产物：
  描述：

  4,4-Dimethyl-6-formylcyclohex-2-en-1-one 在 磺酰氯 作用下， 以 四氯化碳 为溶剂， 生成 6-chloro-4,4-dimethylcyclohex-2-en-1-one
  参考文献：
  名称：

  氯化2-环烯酮的光化学

  摘要：

  新合成了6-氯-2-环己烯酮3、6和11以及5-氯-2-环戊烯酮15。用化合物3和15在烯烃的光环加成中获得的结果表明，通过在烯酮的α′-位用氯取代弗洛林，降低了氧杂环丁烷与环丁烷的产物比。在分子内的光环加成6中没有形成氧杂环丁烷。化合物11不光加成至烯烃中。新合成的2-氯-3-环己烯酮8和9它们在λ= 366 nm的光下也是光稳定的，但是戊烷中的π-π*激发（λ= 254 nm）导致形成4,4-二甲基环己酮（29）。

  DOI：

  10.1002/hlca.19770600316

文献信息

• Functional group hybrids. Reactivity of .alpha.'-nucleofuge .alpha.,.beta.-unsaturated ketones. 2. Reactions with malonate anion. Concerning the mechanism of the Favorskii rearrangement
  作者：Thomas R. Barbee、Hedeel Guy、Mary Jane Heeg、Kim F. Albizati

  DOI：10.1021/jo00024a015

  日期：1991.11

  The scope and limiations of the reaction of alpha'-nucleofuge alpha,beta-unsaturated ketones with sodium dimethyl malonate has been studied systematically. The substrates with good nucleofuges (halides, mesylate) give cyclopropanols upon reaction with malonate anion by way of a conjugate Favorskii reaction. In reactions with substrates containing the poorer nucleofuge (acetoxy) conjugate addition proceeded without entering the Favorskii manifold. Concerning the mechanism of the Favorskii reaction, it is suggested that the loss of the nucleofuge occurs to give a 2-oxyallyl cation, but that disrotatory ring closure is facile and the only products observed result from nucleophilic trapping of cyclopropanones to yield cyclopropanols in fair to good yield.
• Functional group hybrids. Reactivity of .alpha.'-nucleofuge .alpha.,.beta.-unsaturated ketones. 1. Reactions with organocopper reagents
  作者：Thomas R. Barbee、Kim F. Albizati

  DOI：10.1021/jo00024a014

  日期：1991.11

  A series of alpha-nucleofuge alpha',beta'-unsaturated ketones encompassing a variety of structural types and nucleofuges was prepared. Treatment of these compounds with lithium dimethylcuprate or methylcopper leads primarily to either reductive cleavage of the alpha-nucleofuge or conjugate addition. Good alpha-nucleofuges favored the reduction pathway while poorer nucleofuges favored conjugate addition.
• Photochemistry of Chlorinated 2-Cycloalkenones
  作者：Isabelle Altmeyer、Paul Margaretha

  DOI：10.1002/hlca.19770600316

  日期：1977.4.20

  The 6-chloro-2-cyclohexenones 3, 6 and 11, and the 5-chloro-2-cyclopentenone 15 were newly synthesized. The results obtained with compounds 3 and 15 in photocycloadditions to olefins show that the oxetane vs. cyclobutane product ratio is reduced by the substitution of florine by chlorine in the α′ -position of the enone. No oxetanes are formed in the intramolecular photocycloaddition of 6. Compound

  新合成了6-氯-2-环己烯酮3、6和11以及5-氯-2-环戊烯酮15。用化合物3和15在烯烃的光环加成中获得的结果表明，通过在烯酮的α′-位用氯取代弗洛林，降低了氧杂环丁烷与环丁烷的产物比。在分子内的光环加成6中没有形成氧杂环丁烷。化合物11不光加成至烯烃中。新合成的2-氯-3-环己烯酮8和9它们在λ= 366 nm的光下也是光稳定的，但是戊烷中的π-π*激发（λ= 254 nm）导致形成4,4-二甲基环己酮（29）。