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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-12
filingDate 1991-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de733ac84ea216ae868cac94eeab78f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b396dd9647aeba8cb704a2fe957489c5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65dd19566b4b3a016e6405a6e226b7e3
publicationDate 1993-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0550535-A1
titleOfInvention METHOD FOR PRODUCING 2,3-DIFLUOR-6-NITROPHENOL.
abstract According to a process for the production of 2,3-difluor-6-nitrophenol free of isomers, 2,3,4-trifluornitrobenzol is reacted with an aqueous solution of a metal hydroxide of an alkali or alkaline earth metal, in the absence of organic solvent, at temperatures between 20 ° C and 100 ° C approximately, the pH of the reaction mixture is adjusted to a value between 1 and 6 approximately by adding an acid, the product is distilled as well obtained by steam entrainment and 2,3-difluor-6-nitrophenol is isolated, after cooling. Organic solvents are not used during any stage of the process.
priorityDate 1990-09-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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