3,4,5,6-tetrafluorophthaloyldifluoride | 5292-39-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 3,4,5,6-tetrafluorophthaloyldifluoride
• 英文别名: tetrafluorophthaloyl fluoride；Tetrafluor-phthalsaeure-difluorid；3,4,5,6-tetrafluorobenzene-1,2-dicarbonyl Fluoride
• CAS: 5292-39-7
• 化学式: C₈F₆O₂
• 分子量: 242.077
• InChiKey: BCXZYLKBVCDHHC-UHFFFAOYSA-N

物化性质

• 沸点：
  176.0-177.5 °C
• 密度：
  1.644±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为反应物：
  描述：

  3,4,5,6-tetrafluorophthaloyldifluoride 在 溶剂黄146 作用下， 以73.5%的产率得到3,4,5,6-四氟苯酐
  参考文献：
  名称：

  Processes for producing tetrafluorophthalic anhydride and fluorobenzoic

  摘要：

  一种生产四氟邻苯二酐的方法，包括氯化四氯邻苯二酐以得到3,3,4,5,6,7-六氯-1-[3H]-异苯并呋喃酮，然后氟化它以得到3,4,5,6-四氟邻苯二酰二氟化物和/或3,3,4,5,6,7-六氟-1-[3H]-异苯并呋喃酮，然后进一步将四氟邻苯二酰二氟化物和/或六氟-1-[3H]-异苯并呋喃酮与无机碱或有机酸反应以得到四氟邻苯二酐。

  公开号：

  US05523476A1
• 作为试剂：
  描述：

  4-氯-3,5-二硝基三氟甲苯 在 potassium fluoride 、 3,4,5,6-tetrafluorophthaloyldifluoride 作用下， 以 环丁砜 为溶剂， 反应 1.5h， 以79%的产率得到3,4-二氟-5-硝基三氟甲苯
  参考文献：
  名称：

  A general procedure for the fluorodenitration of aromatic substrates

  摘要：

  The synthesis of several fluoroaromatic compounds by a new procedure of fluorodenitration of nitroarenes is reported. The methodology is based on the principle that the nitrite ion, generated during the fluorodenitration processes and responsible for most of the undesired side reactions, can be trapped with a suitable reagent, e.g., phthaloyl difluoride or tetrafluorophthaloyl difluoride. The yields of fluoro compounds thus obtained are good to excellent, and the procedure is of general application.

  DOI：

  10.1021/jo00022a037

文献信息

• Process for producing tetrafluorophthalic anhydride
  申请人：Asahi Glass Company Ltd.

  公开号：US05648504A1

  公开（公告）日：1997-07-15

  A process for producing tetrafluorophthalic anhydride, which comprises chlorinating tetrachlorophthalic anhydride to obtain 3,3,4,5,6,7-hexachloro-1-[3H]-isobenzofuranone, then fluorinating it to obtain 3,4,5,6-tetrafluorophthaloyldifluoride and/or 3,3,4,5,6,7-hexafluoro-1-[3]-isobenzofuranone, and further reacting the tetrafluorophthalolyldifluoride and/or the hexafluoro-1-[3H]-isobenzofuranone with an inorganic base or an organic acid to obtain tetrafluorophthalic anhydride.

  一种生产四氟邻苯二甲酸酐的方法，包括将四氯邻苯二甲酸酐氯化以得到3,3,4,5,6,7-六氯-1-[3H]-异苯并呋喃酮，然后氟化它以得到3,4,5,6-四氟邻苯二甲酰二氟化物和/或3,3,4,5,6,7-六氟-1-[3]-异苯并呋喃酮，然后进一步将四氟邻苯二甲酰二氟化物和/或六氟-1-[3H]-异苯并呋喃酮与无机碱或有机酸反应以得到四氟邻苯二甲酸酐。
• Fluorination process for the production of nuclear fluorinated phthaloyl- and terephthaloyl fluorides
  申请人：IMPERIAL CHEMICAL INDUSTRIES PLC

  公开号：EP0140482A2

  公开（公告）日：1985-05-08

  Nuclear fluorinated phthaloyl and terephthaloyl fluorides, especially tetrafluoroterephthaloyl fluoride, are obtained by reacting a corresponding nuclear chlorinated acid halide with potassium fluoride in a polar aprotic solvent, preferably sulpholane, at a temperature of from 100 to 200°C, preferably 120 to 150°C. The products are useful chemical intermediates for the synthesis of pesticides.

  核氟化邻苯二甲酰基和对苯二甲酰基氟化物，特别是四氟对苯二甲酰基氟化物，是通过在极性非丙烷溶剂（最好是磺烷）中，在 100 至 200℃，最好是 120 至 150℃的温度下，使相应的核氯化酸卤化物与氟化钾反应而得到的。 这些产品是合成杀虫剂的有用化学中间体。
• Process for producing tetrafluorophihalic acid
  申请人：SDS Biotech K.K.

  公开号：EP0259663A1

  公开（公告）日：1988-03-16

  A process for producing tetrafluorophthalic acid is disclosed, which comprises the steps of: (a) reacting an alkali metal fluoride and at least one imide compound represented by formula (I) or (II) wherein X¹, X², X³, and X⁴, which may be the same or different, each represents a chloride atom or a bromide atom, R¹ represents a monovalent organic group, and R² represents a divalent organic group, to provide an N-­substituted tetrafluorophthalimide; and (b) hydrolyzing the tetrafluorophthalimide in the presence of an acid.

  本发明公开了一种生产四氟邻苯二甲酸的工艺，该工艺包括以下步骤：(a) 碱金属氟化物与至少一种由式(I)或(II)代表的亚胺化合物反应，其中 X¹、X²、X³和 X⁴可以相同或不同，各自代表氯原子或溴原子，R¹代表一价有机基团，R²代表二价有机基团，以提供 N-取代的四氟邻苯二甲酰亚胺；以及(b) 在酸存在下水解四氟邻苯二甲酰亚胺。
• Processes for producing tetrafluorophtahlic anhydride and fluorobenzoic acids
  申请人：ASAHI GLASS COMPANY LTD.

  公开号：EP0669310A1

  公开（公告）日：1995-08-30

  A process for producing tetrafluorophthalic anhydride, which comprises chlorinating tetrachlorophthalic anhydride to obtain 3,3,4,5,6,7-hexachloro-1-[3H]-isobenzofuranone, then fluorinating it to obtain 3,4,5,6-tetrafluorophthaloyldifluoride and/or 3,3,4,5,6,7-hexafluoro-1-[3H]-isobenzofuranone, and further reacting the tetrafluorophthalolyldifluoride and/or the hexafluoro-1-[3H]-isobenzofuranone with an inorganic base or an organic acid to obtain tetrafluorophthalic anhydride.

  一种生产四氟邻苯二甲酸酐的工艺，包括将四氯邻苯二甲酸酐氯化以获得 3,3,4,5,6,7-六氯-1-[3H]-异苯并呋喃酮，然后将其氟化以获得 3,4,5,6-四氟邻苯二甲酸二氟化物和/或 3、3,4,5,6,7-六氟-1-[3H]-异苯并呋喃酮，再将四氟邻苯二氟化物和/或六氟-1-[3H]-异苯并呋喃酮与无机碱或有机酸反应，得到四氟邻苯二甲酸酐。
• Processes for producing tetra-fluorophthalic anhydride and fluorobenzioc acids
  申请人：ASAHI GLASS COMPANY LTD.

  公开号：EP0866050A1

  公开（公告）日：1998-09-23

  A process for producing tetrafluorophthalic anhydride, which comprises chlorinating tetrachlorophthalic anhydride to obtain 3,3,4,5,6,7-hexachloro-1-[3H]-isobenzofuranone, then fluorinating it to obtain 3,4,5,6-tetrafluorophthaloyldifluoride and/or 3,3,4,5,6,7-hexafluoro-1-[3H]-isobenzofuranone, and further reacting the tetrafluorophthalolyldifluoride and/or the hexafluoro-1-[3H]-isobenzofuranone with an inorganic base or an organic acid to obtain tetrafluorophthalic anhydride.

  一种生产四氟邻苯二甲酸酐的工艺，包括将四氯邻苯二甲酸酐氯化以获得 3,3,4,5,6,7-六氯-1-[3H]-异苯并呋喃酮，然后将其氟化以获得 3,4,5,6-四氟邻苯二甲酸二氟化物和/或 3、3,4,5,6,7-六氟-1-[3H]-异苯并呋喃酮，再将四氟邻苯二氟化物和/或六氟-1-[3H]-异苯并呋喃酮与无机碱或有机酸反应，得到四氟邻苯二甲酸酐。