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filingDate 1993-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b742dd390ad2054869b662361d4e67ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e8ec8bd348c319162dd1166acbdc9a3c
publicationDate 1993-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0564984-A2
titleOfInvention Process for the preparation of O-iminooxymethylbenzoic acid
abstract m eine ganze Zahl von 0 bis 3 bedeutet X Alkyl; Alkoxy, Nitro, Cyano, Halogen bedeutet R i , R 2 Wasserstoff, Cyano, Hydroxy, Alkyl, Cycloalkyl, Alkenyl, Cycloalkenyl, Alkinyl, Alkoxy, Alkylthio, Benzylthio, Benzylamino, Alkylcarbonyl, ggf. subst. Phenylcarbonyl, ggf. subst. Benzylcarbonyl, Alkoxycarbonyl, ggf. subst. Phenoxycarbonyl, ggf. subst. Benzyloxycarbonyl, ggf. subst. Aryl, ggf. subst. Aryloxy, ggf. subst. Arylthio, ggf. subst. Arylalkyl, ggf. subst. Arylalkenyl, ggf. subst. Aryloxyalkyl, ggf. subst. Arylthioalkyl, ggf. subst. Hetaryl, ggf. subst. Hetaryloxy, ggf. subst. Hetarylthio, ggf. subst. Heteroarylalkyl, ggf. subst. Hetarylalkenyl, ggf. subst. Hetaryloxyalkyl, Hetarylthioalkyl ggf. subst. Heterocyclyl, ggf. subst. Heterocyclyloxy bedeuten, oder N (R 6 ) 2 bedeuten, wobei R 6 H, Alkyl oder Phenyl bedeutet, oder -CO-N(R 7 ) 2 bedeuten, wobei R 7 H, Alkyl oder Phenyl bedeutet, oder R 1 und R 2 zusammen mit dem C-Atom, dessen Substituenten sie sind, einen carbo- oder heterocyclischen Ring bilden können, oder R 1 oder R 2 Halogen bedeutet oder die Gruppen den Restn bedeutet, wobei n die ganzen Zahlen 1 bis 4 bedeutet und die Reste R 8 H, Halogen, Cyano, Nitro; Alkyl, Alkoxy, Aryl, Aryloxy, Benzyloxy, Hetaryl, Hetaryloxy bedeuten, indem man ein Oxim der allgemeinen Formel II,n in dem Ri, R 2 die oben genannte Bedeutung haben, mit einem Lacton der allgemeinen Formel III,n in dem X und m die oben genannte Bedeutung haben, gegebenenfalls in Gegenwart einer Base oder eines Verdünnungsmittels umsetzt und o-Iminooxymethylbenzoesäuren der obengenannten Formel. Process for the preparation of an o-iminooxymethylbenzoic acid of the general formula I. in the m represents an integer from 0 to 3 X alkyl; Alkoxy, nitro, cyano, halogen means R i , R 2 hydrogen, cyano, hydroxy, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, alkoxy, alkylthio, benzylthio, benzylamino, alkylcarbonyl, optionally subst. Phenylcarbonyl, optionally subst. Benzylcarbonyl, alkoxycarbonyl, optionally subst. Phenoxycarbonyl, optionally subst. Benzyloxycarbonyl, optionally subst. Aryl, if necessary subst. Aryloxy, optionally subst. Arylthio, possibly subst. Arylalkyl, optionally subst. Arylalkenyl, optionally subst. Aryloxyalkyl, optionally subst. Arylthioalkyl, optionally subst. Hetaryl, possibly subst. Hetaryloxy, optionally subst. Hetarylthio, possibly subst. Heteroarylalkyl, optionally subst. Hetarylalkenyl, optionally subst. Hetaryloxyalkyl, hetarylthioalkyl optionally subst. Heterocyclyl, optionally subst. Heterocyclyloxy mean, or N is (R 6 ) 2 , where R 6 is H, alkyl or phenyl, or -CO-N (R 7 ) 2 , where R 7 is H, alkyl or phenyl, or R 1 and R 2 together with the C atom, the substituents of which they are, can form a carbocyclic or heterocyclic ring, or R 1 or R 2 is halogen or the group the rest means where n denotes the integers 1 to 4 and the radicals R 8 H, halogen, cyano, nitro; Alkyl, alkoxy, aryl, aryloxy, benzyloxy, hetaryl, hetaryloxy mean by using an oxime of the general formula II, in which R 1, R 2 have the meaning given above, with a lactone of the general formula III, in which X and m have the meaning given above, optionally in the presence of a base or a diluent, and o-iminooxymethylbenzoic acids of the above formula.
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