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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
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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

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