p-C6H4(C(O)Br)2 | 10577-90-9

• 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: p-C6H4(C(O)Br)2
• 英文别名: terephthaloyl bromide；Terephthaloylbromid；Terephthalsaeure-dibromid；Terephthalylbromid；Terephtalsaeurebromid；benzene-1,4-dicarbonyl bromide
• CAS: 10577-90-9
• 化学式: C₈H₄Br₂O₂
• 分子量: 291.927
• InChiKey: PIVFDRVXTFJSIW-UHFFFAOYSA-N

物化性质

• 熔点：
  85 °C(Solv: ligroine (8032-32-4))
• 沸点：
  357.0±25.0 °C(Predicted)
• 密度：
  2.001±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  12
• 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：
  2

反应信息

• 作为反应物：
  描述：

  p-C6H4(C(O)Br)2 、 2-(2-Propylpyrrolidin-1-yl)ethanamine 以 四氢呋喃 为溶剂， 以76%的产率得到N,N'-Bis-[2-(2-propyl-pyrrolidin-1-yl)-ethyl]-terephthalamide; hydrobromide
  参考文献：
  名称：

  Salts of N,N'-bis-[β-2-alkylpyrrolidino)ethyl]phthalamides and their biological action

  摘要：

  DOI：

  10.1007/bf00779275
• 作为产物：
  描述：

  对苯二甲酰氯 在 氢溴酸 作用下， 生成 p-C6H4(C(O)Br)2
  参考文献：
  名称：

  305.邻苯二甲酰溴的互变异构

  摘要：

  DOI：

  10.1039/jr9330001309

文献信息

• METHOD FOR PRODUCING DIHYDROXYBENZENE DERIVATIVE
  申请人：Nagatomo Akinori

  公开号：US20110004013A1

  公开（公告）日：2011-01-06

  A method of producing a compound represented by the following general formula (3): [wherein R is a bivalent aliphatic group having a carbon number of 1-16 or a bivalent aromatic group], which comprises a step (i) of reacting a compound represented by the following general formula (1): with a carboxylic acid halide represented by the following general formula (2): [wherein R is a bivalent aliphatic group having a carbon number of 1-16 or a bivalent aromatic group and X is a halogen atom] in the presence of a basic compound to form an ester, and a step (ii) of conducting a heat treatment after the step (i) to decompose an oligomer in the ester.

  生产以下通用式（3）所代表的化合物的方法：[其中R是具有1-16个碳原子数的二价脂肪族基或二价芳香族基]，包括以下步骤：（i）将以下通用式（1）所代表的化合物与以下通用式（2）所代表的羧酸卤化物在碱性化合物存在下反应形成酯，以及（ii）在步骤（i）之后进行热处理以分解酯中的寡聚体。
• Process for making triazine UV absorbers using lewis acids and reaction promoters
  申请人：CYTEC Technologies Corp.

  公开号：US20010020094A1

  公开（公告）日：2001-09-06

  It has been now surprisingly discovered after extensive research that 2-halo-4,6-bisaryl-1,3,5-triazine can be prepared with unprecedented selectivity, efficiency, mild conditions, and in high yield by the reaction of cyanuric halide with aromatics in the presence of at least one Lewis acid and at least one reaction promoter. This reaction is also unprecedently general as a variety of aromatics can be used to produce a wide selection of 2-halo-4,6-bisaryl-1,3,5-triazines. The novel approach includes the use of the reaction promoters in combination with at least one Lewis acid under certain reaction conditions to promote the formation of 2-halo-4,6-bisaryl-1,3,5-triazine compounds from cyanuric halide. Preferably, the Lewis acids and reaction promoters are combined to form a complex. 2-Halo-4,6-bisaryl-1,3,5-triazines are key intermediates for making 2-(2-oxyaryl)-4,6-bisaryl-1,3,5-triazine class of UV absorbers.

  经过广泛的研究，令人惊讶地发现，通过氰尿酸卤化物与芳香族化合物在至少一种路易斯酸和至少一种反应促进剂的存在下反应，可以以前所未有的选择性、效率、温和条件和高产率制备2-卤代-4,6-双芳基-1,3,5-三嗪。该反应具有前所未有的广泛性，因为可以使用各种芳香族化合物来生产各种2-卤代-4,6-双芳基-1,3,5-三嗪。新的方法包括在特定反应条件下，将反应促进剂与至少一种路易斯酸结合使用，促进从氰尿酸卤化物中形成2-卤代-4,6-双芳基-1,3,5-三嗪化合物。最好将路易斯酸和反应促进剂组合形成复合物。2-卤代-4,6-双芳基-1,3,5-三嗪是制备2-(2-氧基芳基)-4,6-双芳基-1,3,5-三嗪类紫外线吸收剂的关键中间体。
• Processes using alpha, omega-difunctional aldaramides as monomers and crosslinkers
  申请人：Andrews Allen Mark

  公开号：US20060264672A1

  公开（公告）日：2006-11-23

  Processes using alpha, omega-difunctional aldaramides as monomers and crosslinkers are disclosed. The processes can be used to form polymers, particularly crosslinked polymers.

  本发明公开了使用α，ω-双官能团醛胺作为单体和交联剂的过程。该过程可用于形成聚合物，特别是交联聚合物。
• Aromatic amide block copolymer and process of producing the same
  申请人：Miyata Hiroshi

  公开号：US20050090639A1

  公开（公告）日：2005-04-28

  An aromatic amide block copolymer containing a specific aromatic amide compound unit and having a weight average molecular weight, as reduced into standard polystyrene measured by the gel permeation chromatography, of from 10,000 to 1,000,000.

  这是一种芳香酰胺嵌段共聚物，包含特定的芳香酰胺化合物单元，并且其重量平均分子量，以凝胶渗透色谱法测量后转化为标准聚苯乙烯，范围在10,000至1,000,000之间。
• Process for making triazine UV absorbers using Lewis acids and reaction promoters
  申请人：CYTEC Industries Corp.

  公开号：US20020013463A1

  公开（公告）日：2002-01-31

  It has been now surprisingly discovered after extensive research that 2-halo-4,6-bisaryl-1,3,5-triazine can be prepared with unprecedented selectivity, efficiency, mild conditions, and in high yield by the reaction of cyanuric halide with aromatics in the presence of at least one Lewis acid and at least one reaction promoter. This reaction is also unprecedently general as a variety of aromatics can be used to produce a wide selection of 2-halo-4,6-bisaryl-1,3,5-triazines. The novel approach includes the use of the reaction promoters in combination with at least one Lewis acid under certain reaction conditions to promote the formation of 2-halo-4,6-bisaryl-1,3,5-triazine compounds from cyanuric halide. Preferably, the Lewis acids and reaction promoters are combined to form a complex. 2-Halo-4,6-bisaryl-1,3,5-triazines are key intermediates for making 2-(2-oxyaryl)-4,6-bisaryl-1,3,5-triazine class of UV absorbers.

  经过广泛的研究，惊人地发现了一种前所未有的选择性、效率、温和条件和高产率的方法，通过氰尿酸卤化物与芳香族化合物在至少一种路易斯酸和至少一种反应促进剂的存在下反应，制备2-卤代-4,6-双芳基-1,3,5-三嗪。这种反应也是前所未有的普适性，因为可以使用各种芳香族化合物来产生广泛的2-卤代-4,6-双芳基-1,3,5-三嗪选择。新方法包括在特定反应条件下使用反应促进剂与至少一种路易斯酸相结合，促进从氰尿酸卤化物中形成2-卤代-4,6-双芳基-1,3,5-三嗪化合物。最好是将路易斯酸和反应促进剂组合成复合物。2-卤代-4,6-双芳基-1,3,5-三嗪是制造2-(2-氧基芳基)-4,6-双芳基-1,3,5-三嗪类紫外线吸收剂的关键中间体。