http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6016956-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6cfc033f059d282fcd915bc8be2ae53f
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C221-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C225-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44
filingDate 1983-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ef00d60ccbd122266334c8968452718
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07acd45dd1c4cc155e030a761f04a8b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aad937183d2ecc9440ae4151d036a911
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_52e976728f45b457e3ae669fbc44025f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a2257ce3a552cca415e968d2ddd41f3
publicationDate 1985-01-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6016956-A
titleOfInvention Production of 3,3' -or 3,4'-diaminobenzophenone
abstract PURPOSE: To produce the titled compound useful as a raw material of agricultural chemicals and pharmaceuticals, an intermediate of dyes, etc., in high yield, by reducing a benzophenone compound with formic acid or a formic acid salt in the presence of palladium catalyst, and dechlorinating the reduction product. n CONSTITUTION: The objective 3,3'- or 3,4'-diaminobenzophenone is produced by reducing the benzophenone compound of formula (X is Cl substituted to 4 or 6 position; Y is H or Cl, when Y is H, the position of the amino group is 3' or 4', and when Y is 4'-Cl, the amino group is 3') with formic acid or a formic acid salt in the presence of a palladium catalyst (e.g. palladium activated carbon), and dechlorinating the reaction product. The amount of the catalyst is 0.01W10wt% based on the benzophenone compound used as the raw material. The formic acid or the formic acid salt is used in the form of an aqueous solution, and its amount is slight excess to the stoichiometric amount. The solvent is usually the one miscible with water, e.g. alcohol. The reaction is carried out usually at 30W110°C. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1983-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407631466
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3102
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558592
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23938
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415851903
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226497766
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID148536
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID284
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226407820
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635

Total number of triples: 34.