Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e2ed31ee9354301da12dc9a7e9e03df1 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2602-08 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C11B9-0073 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C49-792 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C11B9-008 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-92 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-78 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-94 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-92 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C11B9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-792 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-46 |
filingDate |
1979-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a85ab069495674d1f32ee57f28082749 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26bb3a170b428f0f564fbb5e6ed07ff2 |
publicationDate |
1979-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
EP-0004914-A1 |
titleOfInvention |
Process for the production of compounds useful in perfumery |
abstract |
Process for producing compounds useful in perfumery including isochromans and acylated indane hydrocarbons by reacting the corresponding substituted benzene with an alkylene oxide or with a lower acyl halide in the presence of a hydrocarbon or hydrocarbon mixture containing C 5 to C 10 alkanes at a temperature of at least -20°C; preferably up to -5°C. In the case of forming isochromans, the resulting alcohol is reacted, in situ, with a lower alkanol and a formaldehyde precursor at temperatures of from 20°C up to 80°C. |
isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0089207-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4515990-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8303247-A1 |
priorityDate |
1978-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |