1,1-Dibromo-6-chloro-3-(3-chloropropyl)-1-hexene | 151860-38-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1,1-Dibromo-6-chloro-3-(3-chloropropyl)-1-hexene
• 英文别名: 1,7-dichloro-4-(2,2-dibromoethenyl)heptane
• CAS: 151860-38-7
• 化学式: C₉H₁₄Br₂Cl₂
• 分子量: 352.924
• InChiKey: XPRDULRFQDULJK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5
• 重原子数：
  13
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  1,1-Dibromo-6-chloro-3-(3-chloropropyl)-1-hexene 在 正丁基锂 、 sodium iodide 作用下， 以 四氢呋喃 、 丙酮 为溶剂， 反应 21.0h， 生成 tert-Butyl 7-iodo-4-(3-iodopropyl)-2-heptynoate
  参考文献：
  名称：

  Metal-halogen exchange-initiated intramolecular conjugate addition reactions of conjugated acetylenic esters

  摘要：

  The lithium-iodine exchange-initiated intramolecular conjugate addition reactions of some model gamma-iodo-alpha,beta-acetylenic esters have been examined. Product mixtures arising from proton abstraction reactions were observed in reactions leading to 5-membered ring formation. More efficient cyclizations resulted when reactions were conducted in the presence of trimethylsilyl chloride to trap intermediate allenolate ions. Allenolate ion trapping by an internal electrophilic center in 26 resulted in the highly efficient formation of bicyclic ester 27.

  DOI：

  10.1021/jo00076a053
• 作为产物：
  描述：

  四溴化碳 、 5-Chloro-2-(3-chloropropyl)pentanal 在 三苯基膦 作用下， 以 二氯甲烷 为溶剂， 反应 0.17h， 以72%的产率得到1,1-Dibromo-6-chloro-3-(3-chloropropyl)-1-hexene
  参考文献：
  名称：

  Metal-halogen exchange-initiated intramolecular conjugate addition reactions of conjugated acetylenic esters

  摘要：

  The lithium-iodine exchange-initiated intramolecular conjugate addition reactions of some model gamma-iodo-alpha,beta-acetylenic esters have been examined. Product mixtures arising from proton abstraction reactions were observed in reactions leading to 5-membered ring formation. More efficient cyclizations resulted when reactions were conducted in the presence of trimethylsilyl chloride to trap intermediate allenolate ions. Allenolate ion trapping by an internal electrophilic center in 26 resulted in the highly efficient formation of bicyclic ester 27.

  DOI：

  10.1021/jo00076a053