(S)-3-ethenyl-2-(2-propenyl)-2-cyclohexen-1-ol | 202862-62-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (S)-3-ethenyl-2-(2-propenyl)-2-cyclohexen-1-ol
• 英文别名: (1S)-3-ethenyl-2-prop-2-enylcyclohex-2-en-1-ol
• CAS: 202862-62-2
• 化学式: C₁₁H₁₆O
• 分子量: 164.247
• InChiKey: NTGAJWDWAUMYNR-NSHDSACASA-N

物化性质

• 沸点：
  259.3±29.0 °C(Predicted)
• 密度：
  1.009±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (S)-3-ethenyl-2-(2-propenyl)-2-cyclohexen-1-ol 在 乙酰胺 、 4-二甲氨基吡啶 、 sodium periodate 、 四氧化锇 、 lithium aluminium tetrahydride 、 MMPP 、 二苯基二硒醚 、 双氧水 、 palladium diacetate 、 potassium carbonate 、 N,N-二甲基乙二胺 、 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 、 丙酮 、 叔丁醇 为溶剂， 反应 112.33h， 生成 3-methoxy-7a,9c-(amidoethano)-4a,5,6,7,9c-pentahydrophenanthro[4,5-bcd]furan
  参考文献：
  名称：

  From Chiral ortho-Benzoquinone Monoketals to Nonracemic Indolinocodeines through Diels–Alder and Cope Reactions

  摘要：

  The S-dienol (-)-4 containing 10 carbons and one oxygen of the final product was prepared in 98.6% ee and 39% yield from cyclohexan-1,3-dione. It was attached to the aromatic ring as a monoether of catechol S-(-)-6 and subsequently subjected to oxidative ketalization in methanol. The allylated phenanthrofuran obtained was selectively oxidized at the terminal double bond. The fifth ring was completed by a "one-pot" amidation cyclization process promoted by palladium acetate. The final homochiral indolinocodeine (-)-31 was obtained in 16 steps and 3.6% overall yield from cyclohexan-1,3-dione.

  DOI：

  10.1021/jo3014098
• 作为产物：
  描述：

  3-ethenyl-2-(2-propenyl)-2-cyclohexen-1-one 在 儿萘酚硼烷 、 sodium hydroxide 作用下， 以 甲苯 为溶剂， 反应 19.5h， 以89%的产率得到(S)-3-ethenyl-2-(2-propenyl)-2-cyclohexen-1-ol
  参考文献：
  名称：

  From Chiral ortho-Benzoquinone Monoketals to Nonracemic Indolinocodeines through Diels–Alder and Cope Reactions

  摘要：

  The S-dienol (-)-4 containing 10 carbons and one oxygen of the final product was prepared in 98.6% ee and 39% yield from cyclohexan-1,3-dione. It was attached to the aromatic ring as a monoether of catechol S-(-)-6 and subsequently subjected to oxidative ketalization in methanol. The allylated phenanthrofuran obtained was selectively oxidized at the terminal double bond. The fifth ring was completed by a "one-pot" amidation cyclization process promoted by palladium acetate. The final homochiral indolinocodeine (-)-31 was obtained in 16 steps and 3.6% overall yield from cyclohexan-1,3-dione.

  DOI：

  10.1021/jo3014098