http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103635459-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-24 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C305-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-24 |
| filingDate | 2012-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103635459-B |
| titleOfInvention | The manufacture method of fluorosulfuric acid virtue cyclic esters |
| abstract | Aromatic hydroxylation compound and sulfuryl fluoride (SO is made under the manufacture method of fluorosulfuric acid of the present invention virtue cyclic esters is included in the existence of the tertiary amine except pyridine and picolinen 2 fn 2 ) operation of reacting.The sulfuryl fluoride used in manufacture method of the present invention is widely used as fumigant, easily extensive acquisition.In addition, manufacture method of the present invention can under the reaction conditions of gentleness rapidly and yield obtains target compound well.Manufacture method of the present invention solves the problem of prior art at one stroke, and the industrially preparing process as fluorosulfuric acid virtue cyclic esters is exceedingly useful. |
| priorityDate | 2011-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 57.