http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2017043416-A1
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G02B1-14 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G02B5-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-24 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02B5-30 |
filingDate | 2016-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2018-06-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-WO2017043416-A1 |
titleOfInvention | 2,4,6-tris (2-hydroxy-3-methyl-4-alkoxyphenyl) -1,3,5-triazine compound and 2,4,6-tris (2,4-dihydroxy-3-methylphenyl) ) Method for producing 1,3,5-triazine |
abstract | The object of the present invention is to improve the yield and quality of 2,4,6-tris (2-hydroxy-3-methyl-4-alkoxyphenyl) -1,3,5-triazine compounds and 2,4 , 6-tris (2,4-dihydroxy-3-methylphenyl) -1,3,5-triazine is provided. In the method of the present invention, the reaction between 2,4,6-tris (2,4-dihydroxy-3-methylphenyl) -1,3,5-triazine and an alkylating agent is carried out using a base in the presence of alcohol or water. In addition, an ester compound is used as an additive in the reaction between cyanuric chloride and 2-methylresorcinol. |
priorityDate | 2015-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 218.