http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108997089-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B37-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C37-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C37-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B37-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C39-15 |
| filingDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-108997089-B |
| titleOfInvention | Method for catalyzing arylation of benzyl alcohol compound |
| abstract | The invention belongs to the field of organic synthesis, and discloses a method for catalyzing arylation of a benzyl alcohol compound, which comprises the steps of mixing the benzyl alcohol compound with an aryl compound, adding a solvent and a catalyst of trifluorophenylborane, and reacting for 4-8 hours at 60-120 ℃ to obtain a benzyl alcohol arylation product. The reaction realizes dehydration and arylation reactions on a series of benzyl alcohols by using the trifluoropentafluorophenylborane as a catalyst, and the reaction can quickly construct triarylmethane compounds and organic small molecules containing a plurality of heterocycles, which have important significance in drug molecules. The method is simple to operate, high in reaction efficiency and diverse. |
| priorityDate | 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 54.