http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0025932-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C233-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-14 |
| filingDate | 1980-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0df1c4578d6c980b0def65533ecf954d |
| publicationDate | 1981-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0025932-A1 |
| titleOfInvention | Process for the preparation of 3,3-dimethyl-4-pentene amides |
| abstract | The present invention relates to a process for the preparation of 3,3-dimethyl-pent-4-enoic acid amides of the formula R and R 2 may be the same or different and represent an alkyl radical having 1 to 4 carbon atoms or, together with the nitrogen atom, the substitutions of which they are, form a 5- or 6-membered saturated ring which may also contain a further hetero atom, by reacting acetamide acetals or ketene acetal aminals with 3-methyl-but-2-en-1-ol. The reaction is carried out at a temperature in the range between 80 and 220 ° C, optionally in the presence of an inert organic solvent. The process products are valuable intermediates for the production of insecticidally active cyclopropane carboxylic acid esters. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-4440393-C3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-4440393-A1 |
| priorityDate | 1979-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 89.