3,3-Difluoro-1-iodo-1-(trimethylsilyl)-4-decanone | 169385-17-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3,3-Difluoro-1-iodo-1-(trimethylsilyl)-4-decanone
• 英文别名: 3,3-Difluoro-1-iodo-1-trimethylsilyldecan-4-one
• CAS: 169385-17-5
• 化学式: C₁₃H₂₅F₂IOSi
• 分子量: 390.328
• InChiKey: MZZAFXJOYIUTKI-UHFFFAOYSA-N

物化性质

• 沸点：
  339.0±42.0 °C(Predicted)
• 密度：
  1.275±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  5.23
• 重原子数：
  18
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  3,3-Difluoro-1-iodo-1-(trimethylsilyl)-4-decanone 在 氨 、 水 作用下， 以91%的产率得到4,4-Difluoro-5-hexyl-2-trimethylsilanyl-3,4-dihydro-2H-pyrrole
  参考文献：
  名称：

  Qiu, Zai-Ming; Burton, Donald J., Tetrahedron Letters, 1995, vol. 36, # 29, p. 5119 - 5122

  摘要：

  DOI：
• 作为产物：
  描述：

  1-chloro-1,1-difluoro-2-octanone 在 四(三苯基膦)钯 、 碘 、 锌 作用下， 以 乙腈 为溶剂， 反应 20.5h， 生成 3,3-Difluoro-1-iodo-1-(trimethylsilyl)-4-decanone
  参考文献：
  名称：

  Synthesis of .alpha.,.alpha.-Difluoro-Functionalized Ketones

  摘要：

  In the presence of a catalytic amount of tetrakis(triphenylphosphine) palladium [Pd(PPh(3))(4)], iododifluoromethyl alkyl and phenyl ketones 1 react with alkenes to give the corresponding alpha,alpha-difluoro-gamma-iodo ketones in high yields at room temperature either neat or in hexane at 60 degrees C. A variety of functional groups, such as alkyl, trimethylsilyl, hydroxy, epoxy, ketone, and ester, are tolerated under the reaction conditions. The reaction can be completely suppressed by a radical inhibitor, di-tert-butyl nitroxide or hydroquinone. A ring closure reaction occurs when 1 reacts with diethyl diallylmalonate in the presence of a catalytic amount of Pd(PPh(3))(4). Under UV irradiation, the reaction of 1 with diallyl ether gives a tetrahydrofuran derivative. All these results are consistent with a radical chain mechanism initiated by single electron transfer from Pd(PPh(3))(4) to 1. In the presence of a catalytic amount of nickel dichloride hexahydrate, the iodine in the 1:1 addition adducts is readily reduced by zinc in moist THF under mild conditions to give the corresponding alpha,alpha-difluoro ketones in high yields. A one-pot addition-reduction reaction has been developed for the synthesis of alpha,alpha-difluoro ketones without the isolation of the 1:1 addition adducts, which provides a new, efficient, and practical method for the preparation of a variety of alpha,alpha-difluoro-functionalized ketones.

  DOI：

  10.1021/jo00122a044

文献信息

• A general route to α,α-difluoroketones
  作者：Zai-Ming Qiu、Donald J. Burton

  DOI：10.1016/s0040-4039(00)73671-9

  日期：1993.5

  The reaction of iododifluoromethyl ketones with alkenes catalyzed by Pd(PPh3)4 in the absence of solvent at room temperature gives high yields of the corresponding 1:1 addition products. Treatment of the adducts with Zn/NiCl2.6H2O/THF affords alpha,alpha-difluoroketones. A variety of functional groups in the olefins are tolerated under the reaction conditions, including alkyl, trimethylsilyl, hydroxy, epoxy, carbonyl and ester groups.
• Synthesis of .alpha.,.alpha.-Difluoro-Functionalized Ketones
  作者：Zai-Ming Qiu、Donald J. Burton

  DOI：10.1021/jo00122a044

  日期：1995.9

  In the presence of a catalytic amount of tetrakis(triphenylphosphine) palladium [Pd(PPh(3))(4)], iododifluoromethyl alkyl and phenyl ketones 1 react with alkenes to give the corresponding alpha,alpha-difluoro-gamma-iodo ketones in high yields at room temperature either neat or in hexane at 60 degrees C. A variety of functional groups, such as alkyl, trimethylsilyl, hydroxy, epoxy, ketone, and ester, are tolerated under the reaction conditions. The reaction can be completely suppressed by a radical inhibitor, di-tert-butyl nitroxide or hydroquinone. A ring closure reaction occurs when 1 reacts with diethyl diallylmalonate in the presence of a catalytic amount of Pd(PPh(3))(4). Under UV irradiation, the reaction of 1 with diallyl ether gives a tetrahydrofuran derivative. All these results are consistent with a radical chain mechanism initiated by single electron transfer from Pd(PPh(3))(4) to 1. In the presence of a catalytic amount of nickel dichloride hexahydrate, the iodine in the 1:1 addition adducts is readily reduced by zinc in moist THF under mild conditions to give the corresponding alpha,alpha-difluoro ketones in high yields. A one-pot addition-reduction reaction has been developed for the synthesis of alpha,alpha-difluoro ketones without the isolation of the 1:1 addition adducts, which provides a new, efficient, and practical method for the preparation of a variety of alpha,alpha-difluoro-functionalized ketones.
• Qiu, Zai-Ming; Burton, Donald J., Tetrahedron Letters, 1995, vol. 36, # 29, p. 5119 - 5122
  作者：Qiu, Zai-Ming、Burton, Donald J.

  DOI：——

  日期：——