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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-16
filingDate 1990-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e313288c1b70a32ead59f72127acdfb0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77807211ac0c05aafe529d23c698b795
publicationDate 1991-02-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9101967-A1
titleOfInvention Aqueous reduction process for halo-nitro-phenols
abstract An aminophenolic compound can be synthesized by contacting a halo-nitro-phenolic compound, such as 2-chloro-4,6-dinitroresorcinol, with a hydrogenating agent, such as hydrogen, and a catalyst, such as palladium-on-carbon, in an aqueous solution in the presence of an acid such as phosphoric acid. Reduction in an aqueous medium is safer and more cost-effective than reduction in an organic medium. The acid prevents oxidation of the monomer by oxygen dissolved in the aqueous medium. The process may be used to synthesize aminophenols as 4,6-diaminoresorcinol.
priorityDate 1989-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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