(Z)-3-(1-chloropentylidene)-1-oxaspiro[3.5]nonan-2-one | 849705-14-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 内酯类
• 英文名称: (Z)-3-(1-chloropentylidene)-1-oxaspiro[3.5]nonan-2-one
• 英文别名: (3Z)-3-(1-chloropentylidene)-1-oxaspiro[3.5]nonan-2-one
• CAS: 849705-14-2
• 化学式: C₁₃H₁₉ClO₂
• 分子量: 242.746
• InChiKey: MISDWRLERFDQJY-ZHACJKMWSA-N

物化性质

• 沸点：
  369.2±25.0 °C(Predicted)
• 密度：
  1.13±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.77
• 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：

  (Z)-3-(1-chloropentylidene)-1-oxaspiro[3.5]nonan-2-one 、 正丁基硼酸 在 dichloropalladium;dicyclohexyl-[2-(2,6-dimethoxyphenyl)phenyl]phosphane potassium phosphate 作用下， 以 甲苯 为溶剂， 反应 3.0h， 以37%的产率得到3-(1-butylpentylidene)-1-oxaspiro[3.5]nonan-2-one
  参考文献：
  名称：

  α-氯亚烷基-β-内酯和β-内酰胺与有机硼酸的高效铃木偶联反应

  摘要：

  报道了通过铃木交叉偶联反应活化（Z）-α-氯亚烷基-β-内酯和（E）-α-氯亚烷基-β-内酰胺的CCl键。烷基，杂芳族，取代的苯基和烯基硼酸可以在短时间内以优异的产率与各种α-氯亚烷基-β-内酯和β-内酰胺偶联。光学活性底物的交叉偶联反应导致光学活性化合物没有相应手性中心的外消旋化。

  DOI：

  10.1002/adsc.200600234
• 作为产物：
  描述：

  1-己炔 在 palladium dichloride 正丁基锂 、 对苯醌 、 copper dichloride 作用下， 以 四氢呋喃 为溶剂， -78.0~30.0 ℃ 、2.03 MPa 条件下， 反应 2.0h， 生成 (Z)-3-(1-chloropentylidene)-1-oxaspiro[3.5]nonan-2-one
  参考文献：
  名称：

  Studies on Pd(II)-Catalyzed Synthesis of (Z)-α-Haloalkylidene-β-lactones from Cyclocarbonylation of 2-Alkynols and the Subsequent Coupling Reactions

  摘要：

  A good regio- and stereoselectivity was observed for the PdCl2-catalyzed cyclocarbonylation of 2-alkynols with CuCl2 affording (Z)-alpha-chloroalkylidene-beta-lactons. The highly optically active (Z)-alpha-chloroalkylidene-beta-lactones could be easily prepared from the readily available optically active propargylic alcohols. The Pd(II)-catalyzed cyclocarbonylation of 2-alkynols with CuBr2 was also studied. Although the yields of (Z)-alpha-bromoalkylidene-beta-lactones were low, due to the relatively higher activity of the C-Br bond, the coupling reactions of (Z)-alpha-bromoalkylidene-beta-lactones were quite smooth to afford the corresponding products in high yields. A rationale for this reaction is discussed.

  DOI：

  10.1021/jo0480038

文献信息

• Studies on Pd(II)-Catalyzed Synthesis of (<i>Z</i>)-α-Haloalkylidene-β-lactones from Cyclocarbonylation of 2-Alkynols and the Subsequent Coupling Reactions
  作者：Shengming Ma、Bin Wu、Xuefeng Jiang、Shimin Zhao

  DOI：10.1021/jo0480038

  日期：2005.4.1

  A good regio- and stereoselectivity was observed for the PdCl2-catalyzed cyclocarbonylation of 2-alkynols with CuCl2 affording (Z)-alpha-chloroalkylidene-beta-lactons. The highly optically active (Z)-alpha-chloroalkylidene-beta-lactones could be easily prepared from the readily available optically active propargylic alcohols. The Pd(II)-catalyzed cyclocarbonylation of 2-alkynols with CuBr2 was also studied. Although the yields of (Z)-alpha-bromoalkylidene-beta-lactones were low, due to the relatively higher activity of the C-Br bond, the coupling reactions of (Z)-alpha-bromoalkylidene-beta-lactones were quite smooth to afford the corresponding products in high yields. A rationale for this reaction is discussed.
• Highly Efficient Suzuki Coupling Reaction of α-Chloroalkylidene-β-lactones and β-Lactams with Organoboronic Acids
  作者：Shengming Ma、Xuefeng Jiang、Xin Cheng、Hairong Hou

  DOI：10.1002/adsc.200600234

  日期：2006.10

  -β-lactones and (E)-α-chloroalkylidene-β-lactams via the Suzuki cross-coupling reaction is reported in this paper. Alkyl, heteroaromatic, substituted phenyl- and alkenylboronic acids can be coupled with a wide variety of α-chloroalkylidene-β-lactones and β-lactams in excellent yields within a short period of time. The cross-coupling reaction of optically active substrates leads to the optically active

  报道了通过铃木交叉偶联反应活化（Z）-α-氯亚烷基-β-内酯和（E）-α-氯亚烷基-β-内酰胺的CCl键。烷基，杂芳族，取代的苯基和烯基硼酸可以在短时间内以优异的产率与各种α-氯亚烷基-β-内酯和β-内酰胺偶联。光学活性底物的交叉偶联反应导致光学活性化合物没有相应手性中心的外消旋化。