http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004056736-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_114e4423ec77cbc8dab9d0a98909704e |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-512 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-687 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-51 |
filingDate | 2002-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad88ee9a1958271b3c4e9efe5886372d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb9f79d72e946eeb2222e11883037a60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c80ecb406c2bba067558b8d1f4a406c |
publicationDate | 2004-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | WO-2004056736-A1 |
titleOfInvention | Process for preparing 2,4,4,6-tetrabromo-2,5-cyclohexadienone |
abstract | A highly pure 2,4,4,6-tetrabromo-2,5-cyclohexadienone has been prepared in a single pot, eco-friendly procedure in yields of 91-94 % from phenol. In this method, a mixture of alkali/alkaline earth metal bromide and alkali/alkaline earth metal bromate was employed as brominating agent in place of corrosive liquid bromine. The reaction between phenol and the brominating reagent was initiated by the action of a mineral acid or moderately strong organic acid. The crude product was further characterized by standard analytical and spectroscopic methods. |
priorityDate | 2002-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 37.