METHOD FOR PREPARING 4- AMINOPHENYL- AMINOPHENYL- AMMONIUM- TRIDECYLPHOSPHONATE

Метод за получаване на 4-аминофенил-амониевтридецилфосфонат, характеризиращ се с това,че калциев тридецилфосфонат взаимодействува с аминофенил -амониев сулфат във водна среда, при температура от 0 до 100'с, за предпочитане от 5 до 35'с. Патентните претенции са формулирани в 1 точка The inv...

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Hauptverfasser: GAAL, SANDOR, DUDAR, ERZSEBET, TOTH, BERTALAN, TASNADI, MARTA, KAJATI, ISTVAN, CSERHATI, ILONA, MOLNAR, JANOS, KIS, GYOERGY, EGYHAZI, EVA, CSETE, SANDOR, KOCSIS, MARIA, GOEROEG, KATALIN, VARGA, VALERIA, BODNAR, LASZLO, KAPTAS, TIBOR
Format: Patent
Sprache:bul ; eng
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Zusammenfassung:Метод за получаване на 4-аминофенил-амониевтридецилфосфонат, характеризиращ се с това,че калциев тридецилфосфонат взаимодействува с аминофенил -амониев сулфат във водна среда, при температура от 0 до 100'с, за предпочитане от 5 до 35'с. Патентните претенции са формулирани в 1 точка The invention relates to new compounds of the general formula I (I) wherein R1 is a straight or branched chained alkyl having 1 to 13 carbon atoms, optionally substituted with halogen, alkoxyalkyl containing 1 to 5 carbon atoms in the alkoxy and 1 to 4 carbon atoms in the alkyl moiety or phenyl; R2 is alkyl having 6 to 20 carbon atoms; alkoxyalkyl, phenoxyalkyl, furfuryl, cyclopropyl-alkyl, cyclopentyl, cycloheptyl, thiazolyl, triazolyl, thiazolinyl, pyridinyl, picolyl, benzimidazolyl, piperonyl, pirimidinyl, chlorobenzothiazolyl, benzyl, phenyl substituted with chloro and/or amino, or amino and alkyl, or amino and nitro groups, alkenyl, alkinyl, aminoalkyl, dialkylamino-alkyl, alkylaminoalkyl, alkylphosphonateammoniumalkyl, 3,5-dichlorophenyl-hidantoinyl, or thiadiazolyl optionally substituted with alkyl; R3 is hydrogen, phenyl, benzyl, alkenyl, alkyl, hydroxy, alkoxy or alkoxyalkyl; or R2 and R3 together stand for a 3,5-dichlorophenyl-hidantoinyl group; R4 is hydrogen or alkyl optionally substituted with hydroxyl. The new phosphoric acid monoester salts of the general formula I show fungicidal activity. The fungicidal compositions containing said compounds as active ingredients are also within the scope of the invention. According to a further aspect of the invention there is provided a process for the preparation of the new compounds.