881-99-2Relevant articles and documents
Isophthalic chloride synthesis process (by machine translation)
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Paragraph 0017-0019; 0021; 0023; 0025-0027, (2019/07/04)
The invention relates to a kind of isophthalic chloride synthesis process, steps are as follows: (1) takes xylene, in the 100 - 105 °C to its access excessive COCl2 , By 4 - 10 hours reaction, to obtain the 1, 3 - di (trichloromethyl) benzene thick; (2) taking steps (1) to make the 1, 3 - di (trichloromethyl) benzene thick with the isophthalic acid, in N, N - dimethyl formamide under the catalytic action, 110 - 130 °C reaction 2 - 8 hours, until the non-hydrogen chloride gas is released, the resulting reaction solution obtained by rectification of the isophthalic chloride. The invention has high purity, high yield. The process is simple, raw materials are easy, convenient operation, low cost, easy to treat the exhaust gas, the product quality is high, and the quality is stable, not harmful to the environment and the like, and is suitable for industrial production. (by machine translation)
A second (trichloromethyl) benzene and two (chloroformyl) benzenetrisamide preparation method
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Paragraph 0079; 0080, (2017/02/24)
The present invention relates to a method for preparing bis(trichloromethyl)benzene through a photochemical reaction and preparing bis(chloroformyl)benzene through the further reaction of the bis(trichloromethyl)benzene. According to the present invention, di(methyl)benzene is added to a reactor, chlorine gas is introduced under the control of the illuminance of an incident light source and the reaction temperature, the obtained reaction mixture is subjected to a simple treatment so as to obtain the high purity bis(trichloromethyl)benzene; with the bis(trichloromethyl)benzene of the present invention, the high purity bis(chloroformyl)benzene, one of the aramid fiber production raw materials, can be conveniently obtained; and the preparation method of the present invention has the following advantages that the solvent, the free radical initiator, the photosensitizer and other third components can not be inproduced, and only the stage-control of the reaction condition and the wavelength and the intensity of the light source are required so as to improve the product purity.
METHOD FOR THE PREPARATION OF TRICHLOROMETHYL-GROUP-SUBSTITUTED BENZENE
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Paragraph 0129, (2016/06/28)
The present application relates to a method for photochlorination, and specifically to photochlorination by a photochemical reaction of an aromatic compound with gaseous chlorine so as to prepare a trichloromethyl-substituted benzene, and to a method using bis-(trichloromethyl)-benzene as the trichloromethyl-substituted benzene to prepare by further reaction bis-(chloroformyl)-benzene. Through the control of temperature, illuminance and consumption of gaseous chlorine, the method of this application can greatly improve the purity of trichloromethyl-substituted benzene and further prepare polymer-grade bis-(chloroformyl)-benzene with low cost. The present application also relates to a method for purifying trichloromethyl-substituted benzene, and specifically to a method for purifying trichloromethyl-substituted benzene via molecular distillation. The present application further relates to a photochlorination reactor for use in photochlorination reactions (such as those of the present application).