摘要:
2-fluoro-cyclopropylamine is prepared in an advantageous manner by reacting an N-vinyl compound with a carbene of type FXC: (where X=chlorine or bromine) to give the corresponding cyclopropylamine derivative, replacing the radical X in this derivative by hydrogen, by reduction, and finally eliminating the other substituents on the hydrogen atom.
摘要:
The invention relates to new 3-thiocarbarnoylpyrazole derivatives of the formula (I) in which Ar represents in each case optionally substituted phenyl or pyridyl, R1 represents H2N—CS— and R2 and R3 are as defined in the description, to a plurality of processes for their preparation and to their use as pesticides.
摘要:
A process for preparing perfluoroalkoxy(alkylthio)benzenes from perfluorochloroalkoxy(alkylthio)-benzenes by reaction with hydrogen fluoride in the gas phase and in the presence of a catalyst.
摘要:
Halogenated aromatic compounds are prepared by passing esters of halogenoformic acid at temperatures in the range 150.degree. to 600.degree. C. and pressures from 0.1 to 3 bar over a catalyst containing chromium, magnesium, iron, silicon and/or aluminium, wherein if Al.sub.2 O.sub.3 catalysts are used these have been activated with hydrogen halide.
摘要翻译:卤代芳族化合物通过在含有铬,镁,铁,硅和/或铝的催化剂上通过使卤代甲酸的酯在150℃至600℃的温度和0.1至3巴的压力下进行制备,其中如果Al 2 O 3催化剂 使用这些已被卤化氢活化。
摘要:
1,1,1,4,4,4-hexafluoro-chlorobutenes are obtained by pyrolysis of 1,1,1-trifluoro-2,2-dichloroethane. The hexafluoro-chlorobutenes obtained in this way can be converted into hexafluorobutane, a CFC substitute, by hydrogenation.
摘要:
Process for the preparation of .alpha.-alkoxy-.alpha.-trifluoromethyl-arylacetic esters of the formula (I) ##STR1## wherein R is a component selected from the group consisting of C.sub.1 -C.sub.6 -alkyl, C.sub.2 -C.sub.6 -alkenyl, C.sub.3 -C.sub.7 -cycloalkyl, C.sub.6 -C.sub.10 -aryl and C.sub.1 -C.sub.6 -halogenoalkyl, R' is selected from the group consisting of C.sub.1 -C.sub.4 -alkyl, X is selected from the group consisting of halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.2 -C.sub.4 -alkenyl, C.sub.6 -C.sub.10 -aryl or C.sub.1 -C.sub.4 -alkoxy and nitro, and n is zero or an integer from 1 to 3.
摘要:
Chlorinated aromatics are obtained in a simple manner and in particularly good yield if the corresponding chloroformic esters are heated in the liquid phase to 90.degree. to 240.degree. C. in the presence of an inert organic solvent and a catalytic amount of one or more Lewis acids selected from the group consisting of the aluminium halides, iron halides and antimony halides.
摘要:
1,1,1,4,4,4-Hexafluorobutane is prepared by first reacting 1,1,3,4,4-pentachlorobuta-1,3-diene with hydrogen fluoride in the presence of catalysts at 60.degree. to 180.degree. C. to give 1,1,1,4,4,4-hexafluoro-2-chlorobutane, and converting this to 1,1,1,4,4,4-hexafluorobutane. On working up the product of the first stage of the process, it is possible to isolate novel compounds of formula (I):CF.sub.2 X--CH.sub.2 --R (I)in whichX is fluorine or chlorine andR is --CHCl--CF.sub.2 Cl, --CHCl--CFCl.sub.2 or --CCl.dbd.CCl.sub.2.
摘要:
Avoiding hexachlorobutadiene as the starting material, 2-chloro- and 2,3-dichloro-1,1,1,4,4,4-hexafluoro-2-butene are prepared by reacting a chlorobutene derivative of the formula (I)Cl.sub.2 C.dbd.CH-X (I)in whichX represents CCl.dbd.CCl.sub.2 or CCl.sub.2 --CCl.sub.2 H with hydrogen fluoride and chlorine in the presence of a catalyst at temperatures in the range of 50 to 550.degree. C.
摘要:
1,1,1,4,4,4-Hexafluorobutane (R 356) can be obtained in a simple manner and in excellent yields and with excellent selectivities when 1,1,1,4,4,4-hexafluorobutene is reacted in the liquid phase with hydrogen in the presence of a noble metal catalyst.