diethyl 2-(but-1-ynyl)-2-methylcyclopropane-1,1-dicarboxylate | 1431560-04-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: diethyl 2-(but-1-ynyl)-2-methylcyclopropane-1,1-dicarboxylate
• 英文别名: Diethyl 2-but-1-ynyl-2-methylcyclopropane-1,1-dicarboxylate；diethyl 2-but-1-ynyl-2-methylcyclopropane-1,1-dicarboxylate
• CAS: 1431560-04-1
• 化学式: C₁₄H₂₀O₄
• 分子量: 252.31
• InChiKey: QULUDQDQIOITFW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  18
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-nitrocinnamaldehyde 、 diethyl 2-(but-1-ynyl)-2-methylcyclopropane-1,1-dicarboxylate 在 Ca(bis(triflimide))2 、 tert-butylammonium hexafluorophosphate(V) 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 0.33h， 以80%的产率得到
  参考文献：
  名称：

  The Alkynyl Moiety as a Donor for Donor–Acceptor Cyclopropanes

  摘要：

  The first trans-selective [3 + 2]-cycloaddition of a new type of donor acceptor cyclopropane with aldehydes is presented. 2,2-Disubstituted cyclopropanes, bearing an allryne moiety as the sole donor entity, were transformed to highly substituted tetrahydrofurans in the presence of a catalytic amount of Ca(NTf2)(2)/Bu4NPF6. The protocol allows for an easy access to tetrahydrofurans bearing a versatile alkyne substituent at the quarternary 2-position under very mild reaction conditions.

  DOI：

  10.1021/ol400809n
• 作为产物：
  描述：

  重氮丙酸二乙酯 、 2-甲基-1-己烯-3-炔 在 bis{rhodium[3,3'-(1,3-phenylene)bis(2,2-dimethylpropanoic acid)]} 作用下， 以 二氯甲烷 为溶剂， 生成 diethyl 2-(but-1-ynyl)-2-methylcyclopropane-1,1-dicarboxylate
  参考文献：
  名称：

  The Alkynyl Moiety as a Donor for Donor–Acceptor Cyclopropanes

  摘要：

  The first trans-selective [3 + 2]-cycloaddition of a new type of donor acceptor cyclopropane with aldehydes is presented. 2,2-Disubstituted cyclopropanes, bearing an allryne moiety as the sole donor entity, were transformed to highly substituted tetrahydrofurans in the presence of a catalytic amount of Ca(NTf2)(2)/Bu4NPF6. The protocol allows for an easy access to tetrahydrofurans bearing a versatile alkyne substituent at the quarternary 2-position under very mild reaction conditions.

  DOI：

  10.1021/ol400809n