http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5082932-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03F7-022
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-26
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-71
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03F7-022
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-27
filingDate 1989-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_274b1f5a3fb753c3f0488ed30edef948
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b11f8a13707b48c3156d11b37c361819
publicationDate 1992-01-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5082932-A
titleOfInvention Process for preparing substituted 1,2-naphthoquinone-(2)-diazide-4-sulfonic acid esters and their use in a radiation-sensitive mixture
abstract The invention relates to a process for preparing 1,2-naphthoquinone-(2)-diazide-4-sulfonic acid esters of the general formula I ##STR1## which are substituted in at least one of the positions 5, 6, 7 or 8 by R=halogen, alkoxy groups or alkoxycarbonyl groups and in which X denotes an aryl group. The process comprises steps in which n a) suitably substituted β-naphthol is nitrosated, n b) sulfonation with alkali hydrogensulfite and acid in position 4 and reduction are carried out, n c) the naphthalenesulfonic acid derivative is oxidized, n d) the 1,2-naphthoquinone-4-sulfonic acid formed is reacted with toluenesulfonohydrazide in an organic solvent at temperatures from 20° to 100° C., n e) the naphthoquinonediazide compound is converted with chlorosulfonic acid or chlorosulfonic acid/thionyl chloride into the sulfonyl chloride, and f) the sulfonyl chloride is condensed with a phenolic component, a purification of the respective intermediate product by reprecipitation or recrystallization being unnecessary. n The process makes a simple technical procedure possible with good yield. The compounds prepared, in particular the 1,2-naphthoquinone-(2)-diazide-4-sulfonic acid esters substituted by 6-alkoxycarbonyl groups or by 7-alkoxy groups, are used as radiation-sensitive components in radiation-sensitive mixtures.
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