(1-Chloro-5-methyl-hex-5-enylsulfanyl)-benzene | 125115-17-5

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: (1-Chloro-5-methyl-hex-5-enylsulfanyl)-benzene
• 英文别名: (1-chloro-5-methylhex-5-enyl)sulfanylbenzene
• CAS: 125115-17-5
• 化学式: C₁₃H₁₇ClS
• 分子量: 240.797
• InChiKey: XQCMEFPOFYRZPO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (1-Chloro-5-methyl-hex-5-enylsulfanyl)-benzene 在 oxone 、 偶氮二异丁腈 、 三正丁基氢锡 、 间氯过氧苯甲酸 作用下， 以 甲醇 、 二氯甲烷 、 苯 为溶剂， 反应 19.0h， 生成 2-methyl-6-phenylsulfonyl-1-hexene
  参考文献：
  名称：

  Generation and intramolecular cyclization of α-sulfinyl and α-sulfonyl radicals

  摘要：

  alpha-Phenylsulfinyl and alpha-Phenylsulfonyl radicals are generated by the reactions of alpha-chlorosulfoxides and alpha-chlorosulfones with tributyltin hydride, respectively. High reaction concentration (0.2 M) is required to ensure efficient generations of these radicals. The 5-exo-type intramolecular cyclizations of these radicals are studied. The cyclization is most successful when the olefin is terminally substituted with an ester group. The sulfinyl group only induces mild diastereoselectivity on the cyclization. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00472-9
• 作为产物：
  描述：

  5-methylhex-5-enylsulfanylbenzene 在 N-氯代丁二酰亚胺 作用下， 以 四氯化碳 为溶剂， 生成 (1-Chloro-5-methyl-hex-5-enylsulfanyl)-benzene
  参考文献：
  名称：

  Generation and intramolecular cyclization of α-sulfinyl and α-sulfonyl radicals

  摘要：

  alpha-Phenylsulfinyl and alpha-Phenylsulfonyl radicals are generated by the reactions of alpha-chlorosulfoxides and alpha-chlorosulfones with tributyltin hydride, respectively. High reaction concentration (0.2 M) is required to ensure efficient generations of these radicals. The 5-exo-type intramolecular cyclizations of these radicals are studied. The cyclization is most successful when the olefin is terminally substituted with an ester group. The sulfinyl group only induces mild diastereoselectivity on the cyclization. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00472-9

文献信息

• The study of intramolecular free radical cyclization of α-sulfenyl radical
  作者：Yeun-Min Tsai、Fu-Chang Chang、Jimin Huang、Chi-Lung Shiu

  DOI：10.1016/s0040-4039(01)93728-1

  日期：1989.1

  α-Sulfenyl radical can be generated from α-chlorosulfide or dithioacetal. The olefin substituent effect on the intramolecular radical cyclization of this type was studied.

  α-亚硫酰基可以由α-氯硫化物或二硫缩醛产生。研究了烯烃取代基对这种类型的分子内自由基环化的影响。
• TSAI, YEUN-MIN;CHANG, FU-CHANG;HUANG, JIMIN;SHIU, CHI-LUNG, TETRAHEDRON LETT., 30,(1989) N6, C. 2121-2124
  作者：TSAI, YEUN-MIN、CHANG, FU-CHANG、HUANG, JIMIN、SHIU, CHI-LUNG

  DOI：——

  日期：——