1,1,2,2-tetrabromo-3-methyl-3-(2-methoxyethyl)cyclopropane | 170744-57-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1,1,2,2-tetrabromo-3-methyl-3-(2-methoxyethyl)cyclopropane
• CAS: 170744-57-7
• 化学式: C₇H₁₀Br₄O
• 分子量: 429.772
• InChiKey: HNMNLZQCRRAXFZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.02
• 重原子数：
  12.0
• 可旋转键数：
  3.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  9.23
• 氢给体数：
  0.0
• 氢受体数：
  1.0

反应信息

• 作为反应物：
  描述：

  1,1,2,2-tetrabromo-3-methyl-3-(2-methoxyethyl)cyclopropane 在 甲基锂 作用下， 以 乙醚 为溶剂， 以80%的产率得到1,2-dibromo-3-methyl-3-(2-methoxyethyl)cyclopropene
  参考文献：
  名称：

  The generation and trapping of 1,2-Dibromo-3-methylbut-2-en-1-ylidenes

  摘要：

  1,2-Dibromo-3,3-dimerhylcyclopropene, generated by debromination of 1,1,2,2-tetrabromo-3,3-dimethylcyclopropane on reaction with methyllithium, ring-opens at 0-20 degrees C to produce 1,2-dibromo-3-methylbut-2-en-1-ylidene. This is trapped by alkenes to give vinylcyclopropanes. In the case of electron rich alkenes, the stereochemistry is retained in the product, suggesting that a singlet carbene is involved. In the case of alpha,beta-unsaturated esters, ketones or nitriles, the major cyclopropane produced has the vinyl and electron-withdrawing groups cis-related. 3-(2-Methoxy-ethyl)-3-methyl- and 3-(2-bromoethyl)-3-methyl-1,2-dibromocyclopropenes also ring-open at ambient temperature but little stereoselectivity is observed in the trapping of the derived vinyl-carbenes by alkenes. The reaction of 3-(2-hrdroxrethyl)-3-methyl-1,1,2,2-tetrabromocyclopropane with methyl lithium or diethylphosphite and triethylamine does not lead to an isolable cyclo-propene, but instead to Z-1,2-dibromo-3-methylbuta-1,3-diene; quenching with deuterium oxide at low temperature leads to the incorporation of deuterium at C-1.

  DOI：

  10.1016/0040-4020(95)00448-h
• 作为产物：
  描述：

  硫酸二甲酯 、 3-(2-hydroxyethyl)-3-methyl-1,1,2,2-tetrabromocyclopropane 在 sodium hydroxide 、 四丁基碘化铵 作用下， 以 二氯甲烷 为溶剂， 反应 18.0h， 以82%的产率得到1,1,2,2-tetrabromo-3-methyl-3-(2-methoxyethyl)cyclopropane
  参考文献：
  名称：

  The generation and trapping of 1,2-Dibromo-3-methylbut-2-en-1-ylidenes

  摘要：

  1,2-Dibromo-3,3-dimerhylcyclopropene, generated by debromination of 1,1,2,2-tetrabromo-3,3-dimethylcyclopropane on reaction with methyllithium, ring-opens at 0-20 degrees C to produce 1,2-dibromo-3-methylbut-2-en-1-ylidene. This is trapped by alkenes to give vinylcyclopropanes. In the case of electron rich alkenes, the stereochemistry is retained in the product, suggesting that a singlet carbene is involved. In the case of alpha,beta-unsaturated esters, ketones or nitriles, the major cyclopropane produced has the vinyl and electron-withdrawing groups cis-related. 3-(2-Methoxy-ethyl)-3-methyl- and 3-(2-bromoethyl)-3-methyl-1,2-dibromocyclopropenes also ring-open at ambient temperature but little stereoselectivity is observed in the trapping of the derived vinyl-carbenes by alkenes. The reaction of 3-(2-hrdroxrethyl)-3-methyl-1,1,2,2-tetrabromocyclopropane with methyl lithium or diethylphosphite and triethylamine does not lead to an isolable cyclo-propene, but instead to Z-1,2-dibromo-3-methylbuta-1,3-diene; quenching with deuterium oxide at low temperature leads to the incorporation of deuterium at C-1.

  DOI：

  10.1016/0040-4020(95)00448-h