http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S56125365-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_521f09443d0958a71f4de8ae57ab8291 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-48 |
| filingDate | 1980-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b4250aabda0797a43226c11f3489c9d |
| publicationDate | 1981-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S56125365-A |
| titleOfInvention | Isoindolone derivative |
| abstract | NEW MATERIAL:A isoindolone derivative of formula I (R 1 is lower alkyl). n EXAMPLE: 3-Aryl-3-hydroxy-2-methylisoindolinone. n USE: Pesticides, pharmaceuticals, etc. Raw material of various synthetic chemicals. n PROCESS: The compound of formula I can be prepared by irradiating an alkyl phthalimide of formula II and a silylpropene of formula III (R 2 is lower alkyl or phenyl) in a solvent such as acetonitrile, with light e.g. from a 500-W high-pressure mercury lamp. The benzoazepin derivative of formula IV, which is obtained as a by- product, is a novel compound and expected as pesticides, pharmaceuticals, and a raw material of various synthetic chemicals. Although the amount of the silyl propene of formula III is usually 5mol/1mol of the compound of formula II, it is preferable to use in excess. n COPYRIGHT: (C)1981,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002265441-A |
| priorityDate | 1980-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 29.