351-19-9Relevant articles and documents
Preparation Method for 2,2'-Bis(Trifluoromethyl)-4,4'-Diaminobiphenyl
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Paragraph 0024; 0025, (2021/07/20)
The present invention relates to a method for producing 3,3 '- bis 2,2 - diaminobiphenyl by a benzidine rearrangement reaction from' -4 bis hydrazinobenzene in high yield, and more specifically, to dissolve 4 3,3 '-' - bis hydrazinobenzene in (A) organic solvent. (B) The solution prepared in (A) is added dropwise to an inorganic acid solution while maintaining a temperature below 0 °C.30°C. When the (C) titration is completed, less than 0 °C -30°C or less is reacted. 2,2 '- Bis -4, 4' - diaminobiphenyl, which is characterized in that it comprises.
Method for preparing polyimide monomer having low yellow index
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Paragraph 0039; 0050-0051, (2021/11/02)
The present invention chemically synthesizes a polyimide monomer. 10. The synthesized polyimide monomer is introduced into the loading area of the sublimation purification apparatus. - 3 TTTorr under vacuum above sublimation temperature of the synthesized polyimide monomer, followed by recrystallization. Provided is a method for preparing a polyimide monomer having improved yellowness index.
Preparation method of 2,2'-bis(trifluoromethyl)-4,4'-diaminodiphenyl
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Paragraph 0029; 0030; 0032; 0033; 0035; 0036; 0038; 0039, (2019/02/04)
The invention relates to a preparation method of 2,2'-bis(trifluoromethyl)-4,4'-diaminodiphenyl. The preparation method comprises the following steps: synthesizing 3,3'-bis(trifluoromethyl)hydrazo-benzene in an inorganic alkaline aqueous solution by adopting nitrobenzotrifluoride as a raw material, adopting a phase transfer catalyst, a co-catalyst and Pd/C as a catalytic system and adopting aromatic hydrocarbon as a solvent, and performing the re-arrangement reaction on the 3,3'-bis(trifluoromethyl)hydrazo-benzene in an inorganic acid aqueous solution, thus obtaining 2,2'-bis(trifluoromethyl)-4,4'-diaminodiphenyl, wherein the phase transfer catalyst is one or a mixture of more of sodium dodecyl benzene sulfonate, sodium dodecyl sulfate and cetyl trimethyl ammonium bromide, and the co-catalyst is one or a mixture of more of 2,3-dichloro-1,4-naphthoquinone, 2-hydroxyanthraquinone and 2,6-dioxyanthraquinone. The preparation method has the advantages of mild reaction condition, simple process, high product quality and yield, low production cost, environmental friendliness, suitability for continuous production and the like.