期刊文献+

2,2-双(3-苯基-4-羟基苯基)丙烷的合成研究

Studies on synthesis of 2,2-bis(3-phenyl-4-hydroxyphenyl) propane
原文传递
导出
摘要 以邻苯基苯酚和丙酮为原料,盐酸为催化剂,巯基丙磺酸为助催化剂,通过缩合反应合成了2,2-双(3-苯基-4羟基苯基)丙烷(双OPP-A),研究了原料配比、催化剂用量、反应温度、反应时间等因素对反应的影响,通过实验确定了合成双OPP-A的最优条件为:n(邻苯基苯酚):n(丙酮):n(盐酸):n(巯基丙磺酸)=8:2:4:1,反应温度为60℃,反应时间24h,双OPP-A收率达到78.5%,经重结晶纯度达99.2%。产物通过红外光谱和核磁共振等进行了确证。 The 2,2-bis(3-phenyl-4-hydroxyphenyl) propane(bisOPP-A) was synthesized from o-phenylphenol and acetone by using hydrochloric acid as catalyst and 3-mercaptopropanesulfonic acid as catalytic promoter. The effect of molar ratio of starting materials,the reaction temperature and time on the reaction were studied. The optimum conditions for the synthesis of bisOPP-A are as follows:n(o-phenylphenol):n(acetone):n (hydrochloric acid):n(3-mercaptopropanesulfonic acid) =8:2:4:1,reaction temperature is 60℃and reaction time is 24h,and the yield of bisOPP-A is 78.5%,the purity of the product after recrystaUization is 99.2%.The product was assigned by IR and ~1HNMR.
出处 《精细与专用化学品》 CAS 2011年第4期24-26,共3页 Fine and Specialty Chemicals
基金 山东省科技攻关项目资助(2006GG2203001)
关键词 2 2-双(3-苯基-4羟基苯基)丙烷 邻苯基苯酚 双OPP-A 合成 2 2-bis(3-phenyl-4-hydroxyphenyl) propane o-phenylphenol bisOPP-A synthesis
  • 相关文献

参考文献9

  • 1李复生,殷金柱,魏东炜,崔金华,宋光复.聚碳酸酯应用与合成工艺进展[J].化工进展,2002,21(6):395-398. 被引量:74
  • 2Shigematsu K, Nakagawa T, Sakamo'to S. Dihydric phenols [P]. US5151531, 1992-09-29.
  • 3Hikosaka T. Abrasion-resistant polycarbonate resin, their manufacture, their uses, and their use in eleetrophoto-graphic photoreeeptors[P].JP11246659,1999-09-14.
  • 4秦吉臣,谢小莉,曹贤武,瞿金平.有机胺催化双酚A与碳酸二苯酯熔融酯交换动力学的研究[J].高校化学工程学报,2006,20(6):945-950. 被引量:15
  • 5Hikoska T, Honkawa Y, Sakamoto S. Electrophotographic photoreceptor with polysiloxane-polycarbonate protective coating[P]. JP10232503, 1998-09-02.
  • 6Shaw Paul V. Preparation of bisphenol [P]. US4859803, 1989- 08-22.
  • 7村濑裕明,山田光昭,须田康裕,等.芴衍生物的制造方法[P].CN:1617845A,2005-05-18.
  • 8司春燕,林陵,曾崇余.新型聚碳酸酯单体双OPP-A的合成与表征[J].化工时刊,2007,21(4):1-4. 被引量:3
  • 9Shigematsu K, Nakagawa T, Sakamoto H. Production of dihydroxydiaryl compound [P]. JP63145247, 1988-06-17.

二级参考文献20

  • 1黄振豪.聚碳酸酯合成工艺开发的新进展[J].高分子通报,1994(4):248-254. 被引量:6
  • 2Kim Y S,Choi K Y.Kinetics of melt transesterification of diphenyl carbonate and bisphenol-A to polycarbonate with LiOH·H2O catalyst[J].Ind Eng Chem Res,1992,31(9):2118-2127.
  • 3Ignatov V N,Tartari V,Carraro C,et al.New catalysts for bisphenol A polycarbonate melt polymerization,1:Kinetics of melt transesterification of diphenyl carbonate with bisphenol A[J].Macromol Chem Phys,2001,202(9):1941-1945.
  • 4Ignatov V N,Tartari V,Carraro C,et al.New catalysts for bisphenol A polycarbonate melt polymerization,2:Polymer synthesis and characterization[J].Macromol Chem Phys,2001,202(9):1946-1949.
  • 5Schnell H.Chemistry and Physics of Polycarbonates[M].New York:Wiley,1964.
  • 6Akola J,Jones R O.Branching reactions in polycarbonate:A density functional study[J].Macromolecules,2003,36(4):1355-1360.
  • 7Turska E,Wrobel A M.Effects of temperature on a polycondensation in the melt[J].Polymer,1970,11(8):408-414.
  • 8Turska E,Wrobel A M.Kinetics of polycondensation in the melt of 4,4'-isopropylidene diphenol with diphenyl carbonate[J].Polymer,1970,11(8):415-420.
  • 9Bailly Ch,Daoust D,Legras R,et al.Separation of polycarbonate oligomers by high-performance size exclusion and reverse phase liquid chromatography[J].Polymer,1986,27(5):776-782.
  • 10Ravindranath K,Mashelkar R A.Modeling of polyethylene terephthalate reactors:7.MWD considerations[J].Polym Eng Sci,1984,24(1):30-41.

共引文献85

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部