Abstract:
PROBLEM TO BE SOLVED: To provide a method for producing trifluoromethylaniline by a simple and economical way in an excellent yield and purity and in an industrial amount. SOLUTION: This method for producing trifluoromethylaniline advantageously is provided by nitrating benzotrichloride, reacting the obtained nitrobenzotrichloride with anhydrous hydrofluoric acid for converting its trichlomethyl group into trifluoromethyl group, and finally reducing the nitro group.
Abstract:
PROBLEM TO BE SOLVED: To provide a fluorine-containing bisphenol having a linear molecular structure, and especially useful as a starting material for producing a liquid crystal, a polymer and a flame retardant. SOLUTION: This fluorine-containing bisphenol is the one represented by general formula (wherein, R are each independently hydrogen, F, Cl, Br, I, CN, COOR , a 1-4C alkyl, a 1-4C alkoxy, a 1-4C alkylthio, a 1-4C perfluoroalkyl, a 1-4C perfluoroalkoxy, a 1-4C perfluoroalkylthio, a 1-4C polyfluoroalkyl, a 1-4C polyfluoroalkoxy or a 1-4C polyfluoroalkylthio; R is a 1-4C alkyl; and n is an integer of 0-4).
Abstract translation:要解决的问题:提供具有线性分子结构的含氟双酚,并且特别可用作制备液晶的起始材料,聚合物和阻燃剂。 解决方案:该含氟双酚是由通式表示的双酚(其中,R各自独立地为氢,F,Cl,Br,I,CN,COOR 2,1-4C烷基,1-4C烷氧基, 1-4C烷基硫代,1-4C全氟烷基,1-4C全氟烷氧基,1-4C全氟烷硫基,1-4C多氟烷基,1-4C多氟烷氧基或1-4C多氟烷硫基; R 2为1- 4C烷基; n为0-4的整数)。
Abstract:
An oligophosphate of general formula is disclosed. The oligophosphate is suitable as a flame retardant for thermoplastic molding compositions that exhibit a good flame-retardant effect, improved dimensional stability under the effect of heat, a good level of toughness and excellent flowability.
Abstract:
The invention relates to the oligophosphates of the general formula (I), wherein R and R independently represent, individually selectable for every X, hydrogen, halogen, halogen-substituted or halogen-unsubstituted alkyl, alkyl, cycloalkyl, aryl having 1 to 20 carbon atom each, or R and R together with the carbon atom X to which they are bound form the structure of the formula (II) or a cylocalkyl structure substituted or not substituted by halogen, or R or R , on the carbon atom X, also form, together with an R or R on a further carbon atom X', a cyclic structure that is substituted or not substituted by halogen, R to R independently are the same or different and may represent an alkyl having 1 to 10 carbon atoms or halogen, X represents carbon, m is an integer of from 4 to 7, n is an integer of from 1 to 30, y is 0 or 1, and q may independently be the same or different and represent an integer of from 0 to 5. When used in thermoplastic compositions, said oligophosphates have excellent flame-retarding properties, improved thermal stability, a good viscosity level and excellent flowability.
Abstract:
A method for the production of fluorinated benzaldehydes (I) involves hydrogenation of the corresponding fluorinated benzoyl chloride with hydrogen in presence of a supported palladium catalyst and a catalyst moderator. A method for the production of fluorine-containing benzaldehydes of formula (I), in which [Image] n : 1 or 2; R1-R3H, fluorine, chlorine, bromine, or 1-6C alkyl, fluoroalkyl, fluoroalkoxy or fluoroalkylthio, with at least one of these groups being fluorine or a fluorinated group and not more than two of these groups being bromine, 1-6C fluoroalkoxy and/or 1-6C fluoroalkylthio , involves reacting the corresponding aromatic acid chloride (II) (with COCl instead of CHO in formula (I)) with hydrogen in presence of a supported palladium catalyst and a catalyst moderator.
Abstract:
Production of trifluoromethylanilines (I) comprises: (A) nitrating a benzotrichloride (II); (B) reacting the resulting nitrobenzotrichloride with anhydrous hydrofluoric acid (HF) to convert the trichloromethyl group to a trifluoromethyl group; and (C) reducing the nitro group. Production of trifluoromethylanilines of formula (I) comprises:: (A) nitrating a benzotrichloride of formula (II); (B) reacting the resulting nitrobenzotrichloride with anhydrous HF to convert the trichloromethyl group to a trifluoromethyl group; and (C) reducing the nitro group R = H, F, Cl, Br, Me, CH2Cl, CHCl2 or CHO; R = H, F or Cl; provided that the NH2 group is para to the CF3 group when R and R are H.
Abstract:
1,2-Di-(4-hydroxyphenyl)-tetrafluoroethane compounds (I) are new. 1,2-Di-(4-hydroxyphenyl)-tetrafluoroethane compounds of formula (I) are new: R = hydrogen, fluorine, chlorine, bromine, iodine, cyano, COOR , R , OR or SR ; R = 1-4C alkyl, perfluoroalkyl or polyfluoroalkyl; R = 1-4C alkyl; n = 0-4 Independent claims are also included for the following: (1) new ethers of formula (VI); (2) new 1,2-di(4-fluorophenyl)-dichloroethylenes (IV); and (3) methods for preparing (I), (IV) and other intermediates. R , R = benzyl, substituted benzyl, preferably 1-(1-4 C alkyl)benzyl, (substituted) benzhydryl, isopropyl, tert.-butyl or cyclohexyl); and R' = substituted phenyl groups.