http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20000001047-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b828305495e1cdb63947a3a18aa633d1 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C46-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C50-18 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-675 |
filingDate | 1998-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_223cf499e102724728d27bacffcca804 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d64dc37e7d329fb29e762b6dede767b7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_271eca6560c3386f8ca0273688fb8f41 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9a2cfdcde51d0748dba294ea67054382 |
publicationDate | 2000-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | KR-20000001047-A |
titleOfInvention | Method for producing anthraquinones using 1,4-naphthoquinone and 1,3-butadiene |
abstract | In the present invention, 1,4-naphthoquinone and 1,3-butadiene are subjected to the [2 + 4] Diels-Alder reaction using nitrobenzene as a reaction solvent and an oxidizing agent, followed by continuous oxidative dehydrogenation. The present invention relates to a method for producing anthraquinones.n n n 1,3-butadiene, isoprene and 2,3-dimethyl-1,3-butadiene were used as 1,3-butadienes used in the present invention. Nitrobenzene was used in a molar ratio of 2 to 10 with respect to 1,4-naphthoquinone, [2 + 4] Diels-Alder reaction temperature was 100-150 ° C, and oxidative dehydrogenation reaction was in the range of 160-210 ° C. . In the present invention, the yield of anthraquinones was 90% or more. |
priorityDate | 1998-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 41.