(S)-6-(phenylthio)-2-hexanolN | 135191-48-9

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: (S)-6-(phenylthio)-2-hexanolN
• 英文别名: (2S)-6-phenylsulfanylhexan-2-ol
• CAS: 135191-48-9
• 化学式: C₁₂H₁₈OS
• 分子量: 210.34
• InChiKey: VMIZDRUMHQUDIQ-NSHDSACASA-N

物化性质

• 沸点：
  325.1±25.0 °C(Predicted)
• 密度：
  1.04±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  14
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  45.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (S)-6-(phenylthio)-2-hexanolN 在 Oxone 作用下， 以 甲醇 、 水 为溶剂， 反应 21.0h， 以57%的产率得到(S)-(+)-6-(phenylsulfonyl)-2-hexanol
  参考文献：
  名称：

  Taber, Douglas F.; Silferberg, Lee J.; Robinson, Edward D., Journal of the American Chemical Society, 1991, vol. 113, # 17, p. 6639 - 6645

  摘要：

  DOI：
• 作为产物：
  描述：

  6-Phenylsulfanyl-hexan-2-one 在 葡萄糖 作用下， 以 水 为溶剂， 反应 144.0h， 以53%的产率得到(S)-6-(phenylthio)-2-hexanolN
  参考文献：
  名称：

  Applications of highly enantioenriched alcohols bearing a phenylthio group in the preparation of ring compounds. The two-pot synthesis of an enantiopure spiroacetal pheromone bearing three chiral centers

  摘要：

  The new chiron (S)-6-phenylthio-2-hexanol (3) was prepared in high enantiomeric excess by baker's yeast reduction of the corresponding ketone. Enantioenriched alcohols 1, 2 and 3, prepared previously by a similar procedure, or their racemic counterparts, were transformed into ring closed compounds 5-methyl-2-(phenylthio)tetrahydrofuran (9), 6-methyl-2-(phenylthio)tetrahydropyran (10), 2-methyl-1-phenylsulfonyl cyclopropane (14), cyclobutane (15), cyclopentane (16), and a bee pheromone, (2S,6R,8S)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane (20). (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00635-2

文献信息

• Applications of highly enantioenriched alcohols bearing a phenylthio group in the preparation of ring compounds. The two-pot synthesis of an enantiopure spiroacetal pheromone bearing three chiral centers
  作者：Theodore Cohen、Shaojing Tong

  DOI：10.1016/s0040-4020(97)00635-2

  日期：1997.7

  The new chiron (S)-6-phenylthio-2-hexanol (3) was prepared in high enantiomeric excess by baker's yeast reduction of the corresponding ketone. Enantioenriched alcohols 1, 2 and 3, prepared previously by a similar procedure, or their racemic counterparts, were transformed into ring closed compounds 5-methyl-2-(phenylthio)tetrahydrofuran (9), 6-methyl-2-(phenylthio)tetrahydropyran (10), 2-methyl-1-phenylsulfonyl cyclopropane (14), cyclobutane (15), cyclopentane (16), and a bee pheromone, (2S,6R,8S)-2,8-dimethyl-1,7-dioxaspiro[5.5]undecane (20). (C) 1997 Elsevier Science Ltd.
• Taber, Douglas F.; Silferberg, Lee J.; Robinson, Edward D., Journal of the American Chemical Society, 1991, vol. 113, # 17, p. 6639 - 6645
  作者：Taber, Douglas F.、Silferberg, Lee J.、Robinson, Edward D.

  DOI：——

  日期：——