Bayer Aktiengesellschaft

Klaus-Helmut M Uller

Hans-Joachim Santel

Robert R Schmidt

Klaus K Onig

Klaus L Urssen

Joachim Kluth

Kurt Findeisen

Harry Strang

Hans-Jochem Riebel

Peter Babczinski

Markus Lindig

Dieter Feucht

Karl-Heinz Linker

Wilhelm Haas

Ernst R Gesing

Werner Daum

Michael Schwamborn

Heinz-J Urgen Wroblowsky

Peter M Uller

Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen, of the formula ##STR1## in which R.sup.1 represents hydrogen or an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl and aralkyl,

Herbicidal sulphonylaminocarbonyltriazolinones having two substituents

Intermediates for herbicides, the intermediates having the formula ##STR1## in which R is i-propyl, n-butyl, i-buty, s-butyl or cyclopropyl.

Herbicidal substituted triazolinones

Herbicidal sulphonylaminocarbonyltriazolinones of the formula ##STR1## in which R.sup.1 represents hydrogen, hydroxyl or amino, or represents an optionally substituted radical from the series comprising alkyl, alkenyl, alkinyl, cycloalkyl, aralkyl, aryl, alkoxy, alkenyloxy, alkylamino and dialkylamino,

Sulphonylaminocarbonyltriazolinones

Heterocyclically disubstituted sulphonylamino(thio)carbonyl compounds

Alkoxytriazolinones of the general formula (I), ##STR1## in which R.sup.1 and R.sup.2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl,

Process for the preparation of alkoxytriazolinones

Triazolinone intermediates, for herbicidal sulphonylaminocarbonyltriazolines having substituents which are bonded via sulphur, of the formula ##STR1## in which n is 0, and

Intermediates for herbicidal sulphonylaminocarbonyltriazolinones having

##STR1## in which R.sup.1 represents hydrogen, amino, or an optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aralkyl, aryl, alkylamino, cycloalkylamino or dialkylamino radical,

Herbicidal sulphonylaminocarbonyltriazolinones having substituents

Substituted (herbicidally active) sulphonylaminocarbonyltriazolinones of the formula (I) ##STR1## in which R.sup.1 represents hydrogen, hydroxyl or amino, or represents an optionally substituted radical from the group comprising alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkylamino, dialkylamino, cycloalkyl, cycloalkyloxy, cycloalkylamino, cycloalkylalkyl, aryl or arylalkyl,

Process for preparing sulphonylaminocarbonyltriazolinones

7 Herbicidal 5-alkoxy-1,2,4-triazol-3-(thi)ones of the gerneral formula ##STR1## (in which the radicals R.sup.1, R.sup.2, R.sup.3, X and Y have the meanings given in the description), processes for their preparation, and their use as herbicides, and also new intermediates of the formula (II) ##STR2##

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D usseldorf, Germany

Klaus-Helmut M Uller