http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6831179-B2
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8f8532a13d9870d4b10cdfc36a4bb142 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D327-10 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D327-10 |
filingDate | 2001-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2004-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20752ba07b3e3480257a44a8a5c35539 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29c504e77c6f262897719a8338ab5af1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31c224b0752501ab67971715236c72a7 |
publicationDate | 2004-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-6831179-B2 |
titleOfInvention | Process for the stereoselective preparation of insecticide 6,7,8,9,10-10-hexahalo-1,5,5a,6,9,9a-hexadro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide |
abstract | A process for the stereoselective preparation of insecticide 6,7,8,9,10,10-hexahalo-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide of the general formula I:wherein X is a halogen such as fluorine, chlorine or bromine. The process comprises reacting 1,4,5,6,7,7-hexahalo-5-norbornene-2,3-dimethanol of the general formula IV:wherein X is as defined above, with a cyclic sulfite ring forming reagent optionally in an inert organic solvent at ambient to 139° C., wherein the reaction is carried out in the presence of a stereo isomer directing agent comprising an isomer of the compound of the formula I different from the desired isomer. The molar ratio of the stereoisomer directing agent to the dimethanol compound of the formula IV is at least 0.07. |
priorityDate | 2001-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 53.