http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-194147-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9433d383d1922b3df0ca6c182c7d3925
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-06
filingDate 1985-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d34c9f139a954291c28efd2981b1846d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94daa31a90e3661033542d5a5d2f12c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc770bd1301e5d07c467a3d5727f8c34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8f16b2499714df1c9c9a1f7500e4c1e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2df21200adf6232b9562f52ac76220dd
publicationDate 1988-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-194147-B
titleOfInvention Process for the preparation of 2-hydroxy-6-nitro-toluene
abstract The present invention relates to 2-hydroxy-6-nitro-toluene of formula IVnfor the production of toluene nitration, dinitro toluenesnisomeric mixture, the 2,6-dinitro-nToluene reduction followed by 2-amino-6-nitro-toluenenby diazotizing and brewing, such that andinitro toluene is obtained by nitration of toluene.n■ a mixture with sodium hydroxide in the presence of methanolnreacted for a prolonged period of time, the excellent formula (H)nSeparates 2,6-dinitro toluene and then with sodium sulfidenreduced in the presence of ammonium chloride and an2-Amino-nitro-toluene of formula III is 34-56%nsulfuric acid diazotals and then diazonium saltnAt 70-90 ° C and givennin the case of a solution of the diazonium salt to an additional amountnsulfuric acid.
priorityDate 1985-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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