http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111100056-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-46
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0244
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D417-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-30
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 2019-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111100056-B
titleOfInvention Synthetic method for preparing 3-thiophenyl indole compound by oxygen oxidation without transition metal catalysis
abstract The invention relates to a synthetic method for preparing 3-thiophenyl indole compounds by oxygen oxidation without transition metal catalysis. The method comprises the following steps: adding an initiator, substituted indoline and substituted thiophenol into a reaction tube filled with a solvent, adding a riboflavin catalyst and an oxidant, and reacting for 5-80 hours at the temperature of 30-100 ℃ to obtain a 3-thiophenyl indole product. The main innovation point of the method is that the 3-thiophenyl indole product is prepared by oxygen oxidation without using a transition metal catalyst for high-efficiency catalysis, so that heavy metal pollution is avoided. The method has the advantages of greenness, simple and convenient operation, mild conditions, good substrate universality, high reaction yield and selectivity and the like.
priorityDate 2019-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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