http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2728976-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-54
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-54
filingDate 1977-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3d47e4f1d041fc3b3faa1bce476b4952
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a8a7dccc4480d8e4ae6318a3ff48c30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_160d7cd7714eddad90866f227f5d088d
publicationDate 1979-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2728976-A1
titleOfInvention PROCESS FOR THE PREPARATION OF IMIDAZOLES
abstract Prodn. of imidazoles of formula (I) comprises (a) reacting 1,2-diamines of formula (II) with carboxylic acids of formula (III) or (b) dehydrogenating 2-imidazolines of formula (IV), in either case by heating at 300-600 degrees C in the presence of zinc oxide or a mixt. of zinc oxide and aluminium oxide as catalyst: (R1 - R4 = H or an aliphatic, araliphatic, cycloaliphatic or aromatic residue). (I) are intermediates for dyes, plant protection agents, textile aids, polyurethane and epoxy resin catalysts, surfactants and pharmaceuticals (e.g. nitroimidazoles). They can also be used as catalysts for polymerisations and aldol condensations. (I) is obtd. in good yields and purity. The catalysts used are cheap and easily regenerated, and are not significantly poisoned after prolonged use.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0025191-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4340744-A
priorityDate 1977-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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