http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111039905-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8a483df1d4b5ea677dd937c512c750f2 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-64 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-64 |
filingDate | 2018-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80a5970139004680d821153b6cfee200 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7940c5cabd8773dd2881bb4b7c1e8446 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81396341b6e63cc8f32f39801c567766 |
publicationDate | 2020-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-111039905-A |
titleOfInvention | A kind of preparation method of 5-methyl-5-phenyl-4-arylsulfonyl-furan-2(5H)-one compound |
abstract | The invention discloses a preparation method of a 5-methyl-5-phenyl-4-arylsulfonyl-furan-2(5H)-ketone compound. The compound has the structure shown in formula (I), and its The preparation method comprises: under the condition of inert gas in an organic solvent, heating a phenyl diazonium salt and a compound providing sulfur dioxide to generate a phenylsulfonyl radical, the phenylsulfonyl radical and 4-phenylpentane-2,3-di The alkenoic acid is reacted to cyclize, and a single electron transfer occurs with the catalyst Cu(OAc) 2 to obtain 5-methyl-5-phenyl-4-arylsulfonyl-furan- having the structure shown in formula (I). 2(5H)-ketone compound. The method of the invention can synthesize the sulfonyl-containing furan-2(5H)-one compound under very mild and simple conditions, can be used for large-scale industrial preparation, and has good application prospects in scientific research and industrial fields. |
priorityDate | 2018-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 93.