2,2',6,6'-Tetraphenyl-4,4'-(1-methylethylidene)bisphenol | 124786-92-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二芳基庚烷
• 英文名称: 2,2',6,6'-Tetraphenyl-4,4'-(1-methylethylidene)bisphenol
• 英文别名: 4-[2-(4-Hydroxy-3,5-diphenylphenyl)propan-2-yl]-2,6-diphenylphenol
• CAS: 124786-92-1
• 化学式: C₃₉H₃₂O₂
• 分子量: 532.682
• InChiKey: ACWKCNYOCGALDS-UHFFFAOYSA-N

物化性质

• 沸点：
  686.5±55.0 °C(Predicted)
• 密度：
  1.156±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  10.5
• 重原子数：
  41
• 可旋转键数：
  6
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  40.5
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  双酚A 、 2,6-二苯基苯酚 在 甲烷磺酸 作用下， 以 氯仿 为溶剂， 反应 96.0h， 以87%的产率得到2,2',6,6'-Tetraphenyl-4,4'-(1-methylethylidene)bisphenol
  参考文献：
  名称：

  Synthesis of 2,6-Diphenyl-4,4′-(1-methylethylidene)bisphenol and 2,2′,6,6′-Tetraphenyl-4,4′-(1-methylethylidene)bisphenol

  摘要：

  在甲磺酸存在下，4,4′-(1-甲基乙烯基)双酚（2a）与2,6-二苯基苯酚（1b）发生转移烷基化反应，生成2,2′,6,6′-四苯基-4,4′-(1-甲基乙烯基)双酚（2b）或中间产物2,6-二苯基-4,4′-(1-甲基乙烯基)双酚（6），具体取决于酸浓度。

  DOI：

  10.1055/s-1989-27295

文献信息

• Method for the preparation of aromatic chloroformates
  申请人：Davis Charles Gary

  公开号：US20060293535A1

  公开（公告）日：2006-12-28

  A method for preparing an aromatic chloroformate comprising, introducing a mixture of at least one aromatic hydroxyl compound, phosgene, at least one solvent, and at least one organic base into a flow reactor to obtain a unidirectionally flowing reaction mixture. The unidirectionally flowing reaction mixture is maintained at a temperature between about 0° C. and about 60° C. to produce a single product stream comprising an aromatic chloroformate.

  一种制备芳香氯甲酸酯的方法包括，将至少一种芳香羟基化合物、光气、至少一种溶剂和至少一种有机碱的混合物引入流动反应器中，以获得单向流动的反应混合物。将单向流动的反应混合物保持在约0°C至约60°C的温度下，以产生包含芳香氯甲酸酯的单一产物流。
• Method for the preparation of aliphatic chloroformates
  申请人：Davis Charles Gary

  公开号：US20060084822A1

  公开（公告）日：2006-04-20

  A method for preparing an aliphatic chloroformate comprising, introducing a mixture of at least one aliphatic hydroxyl compound, phosgene, at least one solvent, and optionally at least one organic base into a flow reactor to obtain a unidirectional flowing reaction mixture. The at least one aliphatic hydroxyl compound comprises at least one aliphatic hydroxyl group. The unidirectional flowing reaction mixture is maintained at a temperature between about 0° C. and about 60° C. to produce a single product stream comprising an aliphatic chloroformate.

  制备脂肪基氯甲酸酯的方法包括，将至少一种脂肪基羟基化合物、光气、至少一种溶剂以及可选的至少一种有机碱的混合物引入流动反应器中，以获得单向流动的反应混合物。至少一种脂肪基羟基化合物包括至少一种脂肪基羟基。将单向流动的反应混合物保持在约0°C至约60°C的温度下，以产生包含脂肪基氯甲酸酯的单一产物流。
• Sulfonated polyaryletherketone-block-polyethersulfone copolymers
  申请人：Brunelle Daniel Joseph

  公开号：US20080004443A1

  公开（公告）日：2008-01-03

  Sulfonated block copolymer suitable for use as proton exchange membranes for fuel cells comprise sulfonated polyaryletherketone blocks and polyethersulfone blocks. The sulfonated polyaryletherketone blocks comprise structural units of formula I wherein R 1 is C 1 -C 10 alkyl, C 3 -C 12 cycloalkyl, C 6 -C 14 aryl, allyl, alkenyl, alkoxy, halo, or cyano; Ar 1 and Ar 2 are each independently C 6 -C 20 aromatic radicals, or Ar 1 and Ar 2 , taken together with an intervening carbon atom, form a bicyclic C 6 -C 20 aromatic radical or a tricyclic C 6 -C 20 aromatic radical; M is H, a metal cation, a non-metallic inorganic cation, an organic cation or a mixture thereof; and a is 0 or an integer from 1 to 4.

  适用于燃料电池质子交换膜的磺化嵌段共聚物包括磺化聚芳醚酮嵌段和聚醚砜嵌段。磺化聚芳醚酮嵌段包括以下结构单位I的结构单元，其中R1是C1-C10烷基，C3-C12环烷基，C6-C14芳基，烯丙基，烯烷基，烷氧基，卤素或氰基；Ar1和Ar2分别是C6-C20芳香基，或Ar1和Ar2连同一个介于碳原子形成一个双环C6-C20芳香基或三环C6-C20芳香基；M为H，金属阳离子，非金属无机阳离子，有机阳离子或它们的混合物；a为0或1至4之间的整数。
• [EN] METHOD OF BISPHENOL MANUFACTURE<br/>[FR] PROCÉDÉ DE FABRICATION DE BISPHÉNOL
  申请人：SABIC GLOBAL TECHNOLOGIES BV

  公开号：WO2017100164A1

  公开（公告）日：2017-06-15

  An improved method of manufacture of a bisphenol comprises heating a monohydric phenol to a first temperature sufficient to melt the monohydric phenol; adding a carbonyl compound to 2.0-3.0 molar equivalents, based on the moles of carbonyl compound, of the monohydric phenol in the presence of catalytic amounts of an organosulfonic acid catalyst and a reaction promoter at a second temperature sufficient to maintain unreacted monohydric phenol in a molten state; increasing the temperature to a third temperature higher than the second temperature, and mixing for a time sufficient to produce the bisphenol in a yield of 80 to 100%, based on the amount of carbonyl compound; wherein mineral acids, Lewis acids, and ion exchange resins are not used. The method is applicable to the manufacture of 2,2-bis(3,5-dimethyl-4-hydroxyphenyl)propane, a useful intermediate for the manufacture of bifunctional poly(phenylene ether)s.

  一种改进的双酚制造方法包括将一种一元酚加热至足以使其熔化的第一温度；在存在催化量的有机磺酸催化剂和反应促进剂的情况下，向一元酚中加入2.0-3.0摩尔当量的羰基化合物，基于羰基化合物的摩尔数，在足以保持未反应的一元酚处于熔化状态的第二温度；将温度提高至高于第二温度的第三温度，并混合一段足以产生双酚的时间，其收率为80%至100%，基于羰基化合物的数量；其中不使用矿酸、路易斯酸和离子交换树脂。该方法适用于制造2,2-双(3,5-二甲基-4-羟基苯基)丙烷，这是制造双功能聚(苯醚)的有用中间体。
• Methods for producing and purifying 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine monomers and polycarbonates derived therefrom
  申请人：Rai Kumar Vinod

  公开号：US20050288517A1

  公开（公告）日：2005-12-29

  Disclosed herein is a method for producing a 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine. The method comprises forming a reaction mixture comprising at least one substituted or unsubstituted phenolphthalein compound, at least one substituted or unsubstituted primary hydrocarbyl amine, and an acid catalyst; and heating the reaction mixture to form 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine. An adduct of the 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine is formed either by using an excess of the primary hydrocarbyl amine in the first heating step, or by isolating crude 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine after the heating step and then reacting with a further amount of the primary hydrocarbyl amine. The 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine has a formula: where R 1 is selected from the group consisting of a hydrogen and a hydrocarbyl group, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen.

  本文公开了一种制备2-烃基-3,3-双(4-羟基芳基)邻苯二酰亚胺的方法。该方法包括形成一个反应混合物，其中包括至少一种取代或未取代的苯酞化合物、至少一种取代或未取代的一次烃基胺和酸催化剂；并加热反应混合物以形成2-烃基-3,3-双(4-羟基芳基)邻苯二酰亚胺。2-烃基-3,3-双(4-羟基芳基)邻苯二酰亚胺的加合物可通过在第一次加热步骤中使用过量的一次烃基胺来形成，或者通过在加热步骤后分离粗糙的2-烃基-3,3-双(4-羟基芳基)邻苯二酰亚胺然后与进一步的一次烃基胺反应来形成。2-烃基-3,3-双(4-羟基芳基)邻苯二酰亚胺具有以下化学式：其中R1选自氢和烃基团组成的群，R2选自氢、烃基团和卤素组成的群。