Dibut-3-ynyl diselenide | 154414-94-5

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: Dibut-3-ynyl diselenide
• 英文别名: Diselenide, di-3-butynyl；4-(but-3-ynyldiselanyl)but-1-yne
• CAS: 154414-94-5
• 化学式: C₈H₁₀Se₂
• 分子量: 264.087
• InChiKey: IIUDFYLBRIBAGT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.19
• 重原子数：
  10
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.5
• 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：

  2-甲氧基乙氧基甲基氯 、 Dibut-3-ynyl diselenide 在 lithium aluminium tetrahydride 作用下， 生成 3-Butynyl (2-methoxyethoxy)methyl selenide
  参考文献：
  名称：

  A New Method of Generation of .alpha.-Selenocarbenium Ions from Se,O-Heteroacetals and Their Reactions

  摘要：

  Various Se,O-heteroacetals were prepared by the LiAlH4 reduction of diselenides 1 followed by alkylation with methoxymethyl chloride or (2-methoxyethoxy)methyl (MEM) chloride. Olefinic and acetylenic alpha-seleno carbenium ions were generated by the selective C-O bond cleavage of O-(2-methoxyethyl)-Se,O-heteroacetals with titanium(IV) chloride and cyclized to give the seleno heterocyclic compounds. Olefinic MEM-selenides 3a,b,d-f,h underwent the endo-mode cyclization to afford 4-chloroselenacycloalkanes 4a,b,d-f,h in good yields, whereas acetylenic MEM-selenides 12b-e,g-j underwent the exo-mode cyclization to give 3-(1-chloroalkylidene)selenacycloalkanes 13b-e,g-j. This new utilization of alpha-seleno carbenium ions was also applied to the intramolecular and intermolecular Friedel-Crafts reactions.

  DOI：

  10.1021/jo00084a017
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 selenium 、 sodium tetrahydroborate 作用下， 以 乙醇 为溶剂， 生成 Dibut-3-ynyl diselenide
  参考文献：
  名称：

  A New Method of Generation of .alpha.-Selenocarbenium Ions from Se,O-Heteroacetals and Their Reactions

  摘要：

  Various Se,O-heteroacetals were prepared by the LiAlH4 reduction of diselenides 1 followed by alkylation with methoxymethyl chloride or (2-methoxyethoxy)methyl (MEM) chloride. Olefinic and acetylenic alpha-seleno carbenium ions were generated by the selective C-O bond cleavage of O-(2-methoxyethyl)-Se,O-heteroacetals with titanium(IV) chloride and cyclized to give the seleno heterocyclic compounds. Olefinic MEM-selenides 3a,b,d-f,h underwent the endo-mode cyclization to afford 4-chloroselenacycloalkanes 4a,b,d-f,h in good yields, whereas acetylenic MEM-selenides 12b-e,g-j underwent the exo-mode cyclization to give 3-(1-chloroalkylidene)selenacycloalkanes 13b-e,g-j. This new utilization of alpha-seleno carbenium ions was also applied to the intramolecular and intermolecular Friedel-Crafts reactions.

  DOI：

  10.1021/jo00084a017

文献信息

• A New Method of Generation of .alpha.-Selenocarbenium Ions from Se,O-Heteroacetals and Their Reactions
  作者：Mitsuhiro Yoshimatsu、Takashi Sato、Hiroshi Shimizu、Mikio Hori、Tadashi Kataoka

  DOI：10.1021/jo00084a017

  日期：1994.3

  Various Se,O-heteroacetals were prepared by the LiAlH4 reduction of diselenides 1 followed by alkylation with methoxymethyl chloride or (2-methoxyethoxy)methyl (MEM) chloride. Olefinic and acetylenic alpha-seleno carbenium ions were generated by the selective C-O bond cleavage of O-(2-methoxyethyl)-Se,O-heteroacetals with titanium(IV) chloride and cyclized to give the seleno heterocyclic compounds. Olefinic MEM-selenides 3a,b,d-f,h underwent the endo-mode cyclization to afford 4-chloroselenacycloalkanes 4a,b,d-f,h in good yields, whereas acetylenic MEM-selenides 12b-e,g-j underwent the exo-mode cyclization to give 3-(1-chloroalkylidene)selenacycloalkanes 13b-e,g-j. This new utilization of alpha-seleno carbenium ions was also applied to the intramolecular and intermolecular Friedel-Crafts reactions.