177030-60-3Relevant articles and documents
Process for preparing alkoxytriazolinones
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, (2008/06/13)
Alkoxytriazolinones of the formula (I) ?known for example as intermediates for preparing agrochemically active compounds! STR1 wherein R represents an alkyl group, an alkenyl group, an alkinyl group, a cycloalkyl group, a cycloalkylalkyl group, an aryl group or an arylalkyl group, any of which may be substituted, are prepared by reacting a) thioimidodicarboxylic diesters of the general formula (II) STR2 wherein R is as defined above and R1 represents an alkyl group, an arylalkyl group or an aryl group, any of which may be substituted, with b) hydrazine, hydrazine hydrate or an acid adduct of hydrazine. The reaction is conducted i) in the presence of a diluent and, optionally, in the presence of a basic reaction auxiliary, and ii) at temperatures between -10° C. and +100° C.
Process for the preparation of alkoxytriazolinones
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, (2008/06/13)
Alkoxytriazolinones of the formula (I), STR1 in which R1 and R2 independently of one another represent in each case optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, (which can be used as intermediates for the preparation of herbicidal active compounds) are obtained in good yields and in high purity by reacting iminocarbonic diesters (II) with carbazinic esters (III) STR2 in which R2 and R3 in each case represent, for example, alkyl or aryl, at -20° C. to +120° C. (1st step) and subjecting the semicarbazide derivatives (IV) formed in this process with elimination of R2 --OH STR3 to a cyclizing condensation reaction in the presence of a base at 20° C. to 150° C. with elimination of R3 --OH, if appropriate (2nd step) and, finally, by reacting the resulting 5-alkoxytriazolinones of the formula (V) with an alkylating agent of the formula R1 --X (VI) at 0° C. to 150° C., if appropriate in the presence of a base (3rd step: highly selective 4-alkylation).
