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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D335-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B57-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B57-14
filingDate 1980-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bd1bf6bcf4cdbcb7ea9c026a104d09d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b7dc3753ee5c830ad7b0b7b2b15ec9a
publicationDate 1980-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0019872-A1
titleOfInvention Process for the preparation of benzoxanthene and benzothioxanthene dyestuffs
abstract Mixtures of isomers of dyes of the formulas and wherein X is an oxygen or sulfur atom, R is an optionally substituted alkyl radical, acyl radical or benzenesulfonyl radical, R 1 and R 2 are hydrogen or halogen atoms, alkyl, phenyl, acyl, acyloxy, carbalkoxy, alkoxy, nitro, alkylthio or alkylsulfonyl groups or together a fused benzene ring, R 3 and R 4 are hydrogen or halogen atoms, phenyl groups, alkyl, alkoxy, carbalkoxy groups with 1 to 4 carbon atoms or nitrile groups, R 5 and R 6 are hydrogen atoms or optionally substituted alkoxy groups with 1 up to 4 carbon atoms mean are by condensation of the corresponding benzoxanthene or benzothioxanthene-3,4-dicarboxylic acid anhydrides or esters with phenylacetic anhydrides or esters in the presence of alkali at about 150-260 ° C and subsequent alkylation or acylation of the hydroxy compounds thus obtained without them Obtain previous isolation if you carry out condensation and alkylation or acylation in a polar organic solvent.
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priorityDate 1979-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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