http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4943637-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-20
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-20
filingDate 1988-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a8fae2ddd9f3315f5fc47993307b164
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4efd1447b50bd817721b1c3881a3cce
publicationDate 1990-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4943637-A
titleOfInvention Method for preparing 2-phenylbenzotriazoles
abstract This invention relates to a method for preparing a 2-phenylbenzotriazole of formula I, ##STR1## (wherein R 1 represents hydrogen or chlorine atom, a lower alkyl group having a carbon number of 1 to 4, a lower alkoxy group having a carbon number of 1 to 4, carboxyl group, or sulfonic acid group; R 2 represents hydrogen or chlorine atom, a lower alkyl group having a carbon number of 1 to 4, or a lower alkoxy group having a carbon number of 1 to 4; R 3 represents hydrogen or chlorine atom, an alkyl group having a carbon number of 1 to 12, a lower alkoxyl group having a carbon number of 1 to 4, phenyl group, a phenyl group substituted with an alkyl group having a carbon number of 1 to 8, phenoxy group, or a phenylalkyl group, the alkyl part of which has a carbon number of 1 to 4; R 4 represents hydrogen or chlorine atom, hydroxyl group, or a lower alkoxy group having a carbon number of 1 to 4; and R 5 represents hydrogen atom, an alkyl group having a carbon number of 1 to 12, or a phenylalkyl group, the alkyl part of which has a carbon number of 1 to 4), which comprises reducing an o-nitroazobenzene of formula III, ##STR2## (wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined above) with at least one selected from the group consisting of primary and secondary alcohol reducing agents in the presence of an aromatic ketone catalyst and base. n This invention further relates to a method for preparing a 2-phenylbenzotriazole of formula I as defined above, which comprises reducing 1 mole 2-phenylbenzotriazole-N-oxide of formula II, ##STR3## (wherein R 1 , R 2 , R 3 , R 4 and R 5 are as defined above) with 0.4 to 0.7 mole primary alcohol and/or 0.8 to 1.4 mole secondary alcohol in the presence of an aromatic ketone catalyst and base. n This invention still further relates to a method for preparing a 2-phenylbenzotriazole-N-oxide of formula II as defined above, which comprises reducing 1 mole o-nitroazobenzene of formula III as defined above with 0.4 to 0.7 mole primary alcohol and/or 0.8 to 1.4 mole secondary alcohol in the presence of an aromatic ketone catalyst and base.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10976
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226412386
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129443413
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226494866
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234610773
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234611771
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226410094
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID103927
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129940090
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID223740337
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232548483
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20568092
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234611781
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127711810
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128309500
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234611819
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8209
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128243147
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129354638
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234610615

Total number of triples: 310.