http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-999612-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ad66884a6f2a66126d492e56e09be39
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-275
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-32
filingDate 1962-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1965-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-999612-A
titleOfInvention Process for the preparation of basically substituted phenylacetonitriles
abstract Basically substituted phenylacetonitriles of the general formula <FORM:0999612/C2/1> wherein A, B and C represent hydrogen or halogen atoms, or alkyl or alkoxy groups with 1-3 carbon atoms, or A and B or B and C together form a methylene-dioxy group, and at least one of the symbols A, B or C has a meaning other than hydrogen, R represents a hydrogen atom or an alkyl radical with 1-3 carbon atoms, R1 represents a hydrogen atom, an alkyl or alkenyl radical with up to 5 carbon atoms, or a saturated or unsaturated, cyclic or bicyclic hydrocarbon radical, and Alk represents an alkylene group with 2-5 carbon atoms, are obtained by reacting, in the presence of basic condensation agents, a phenylacetonitrile of the formula <FORM:0999612/C2/2> with a compound of the formula <FORM:0999612/C2/3> wherein X represents a reactive acid radical, and subsequently reacting the products wherein R1 represents a hydrogen atom with a compound of the formula R1-X, wherein R1 has a meaning other than hydrogen. Reactive acid radicals include halogen atoms, sulphuric acid radicals in ester-like linking to the organic groups in question or the corresponding benzene or toluene sulphonic acid radicals. Basic condensation agents include sodium amide, lithium amide, and lithium diethylamide.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5457224-A
priorityDate 1961-04-01-04:00^^<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/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447550105
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8794
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24533
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456171974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11137085
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447528836
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7371
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419516690
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425013245
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451412631

Total number of triples: 29.