5-chlorotetrafluorophenol | 14754-08-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 英文名称: 5-chlorotetrafluorophenol
• 英文别名: 2,4,5,6-Tetrafluor-chlorphenol；3-Chlor-tetrafluor-phenol；3-Chlortetrafluorphenol；3-Chloro-2,4,5,6-tetrafluorophenol
• CAS: 14754-08-6
• 化学式: C₆HClF₄O
• 分子量: 200.52
• InChiKey: UBVBZYQWALSEIS-UHFFFAOYSA-N

物化性质

• 沸点：
  178.6±35.0 °C(Predicted)
• 密度：
  1.718±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  2,3,4,5,6-pentafluoro-6-chloro-2,4-cyclohexadienone 、 以 乙醚 为溶剂， 反应 5.0h， 生成 五氟苯酚 、 5-chlorotetrafluorophenol 、 2,4,5,6-tetrafluoro-3-(phenyldiazenyl)phenol
  参考文献：
  名称：

  Formation of polyfluorinated azobenzenes and azophenols in the reactions of chloropentafluoro-cyclohexa-2,5- and -2,4-dienones with phenyl- and pentafluorophenylhydrazines

  摘要：

  4-Chloropentafluorocyclohexa-2,5-dienone reacted with phenyl- and pentafluorophenylhydrazines in the presence of AlCl3 via addition to the carbonyl group with formation of the corresponding azobenzenes. The reaction of 6-chloropentafluorocyclohexa-2,4-dienone with phenyl- and pentafluorophenylhydrazines both in the presence and in the absence of AlCl3 afforded mainly 3-arylazotetrafluorophenols as products of nucleophilic replacement of fluorine atom at the double C=C bond.

  DOI：

  10.1134/s1070428014010060

文献信息

• Process for the preparation of halogenated (meth)acrylic esters and poly (meth) arcylates obtained with said (meth)acrylic esters
  申请人：Akzo Nobel N.V.

  公开号：EP0824096A2

  公开（公告）日：1998-02-18

  The present invention is directed to a process for the preparation of (meth)acrylates of halogenated alcohols by direct esterification of said alcohols with (meth)acrylic acid (chloride) wherein at least 2,6-substituted pyridine derivative is used as a polymerization inhibitor at room temperature or lower. Suitable at least 2,6-substituted pyridine derivatives are 2,6-lutidine, 2,4,6-collidine or 2,6-di-tert.butyl-4-methyl pyridine. With the halogenated (meth)acrylate esters prepared with the process according to the invention, very pure homo- and copolymers can be prepared, resulting in polymers having a low optical loss of 0.1 dB/cm or lower at 1300 nm and lower than 0.4 dB/cm at 1550 nm.

  本发明涉及一种通过将卤代醇与（甲基）丙烯酸（氯化物）直接酯化来制备（甲基）丙烯酸酯的方法，其中至少使用一种2,6-取代吡啶衍生物作为聚合抑制剂，温度为室温或更低。适用的至少2,6-取代吡啶衍生物包括2,6-吡啶、2,4,6-考林或2,6-二叔丁基-4-甲基吡啶。 通过根据本发明的方法制备的卤代（甲基）丙烯酸酯，可以制备非常纯净的同聚物和共聚物，从而得到在1300纳米处光学损耗低至0.1 dB/cm或更低，在1550纳米处低于0.4 dB/cm的聚合物。
• Formation of polyfluorinated azobenzenes and azophenols in the reactions of chloropentafluoro-cyclohexa-2,5- and -2,4-dienones with phenyl- and pentafluorophenylhydrazines
  作者：V. N. Kovtonyuk

  DOI：10.1134/s1070428014010060

  日期：2014.1

  4-Chloropentafluorocyclohexa-2,5-dienone reacted with phenyl- and pentafluorophenylhydrazines in the presence of AlCl3 via addition to the carbonyl group with formation of the corresponding azobenzenes. The reaction of 6-chloropentafluorocyclohexa-2,4-dienone with phenyl- and pentafluorophenylhydrazines both in the presence and in the absence of AlCl3 afforded mainly 3-arylazotetrafluorophenols as products of nucleophilic replacement of fluorine atom at the double C=C bond.