http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5553275-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d3de607e369a55daf2120ea4267a4827
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-10
filingDate 1978-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6eb67a367c15043b0777b1c53b20df74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f16cfaba169ac13835a059926ceff54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4822cb15e0a9970ae3c5b836b7cdd6c7
publicationDate 1980-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5553275-A
titleOfInvention Preparation of substituted 1,2-dihydro-1,3,5-triazine
abstract PURPOSE: To obtain the title substance useful as an intermediate for pesticides, medicines, and high polymers in one step in high yield without using powerful agents, by reacting a nitrile and an aldehyde or ketone in the presence of ammonia and an alcohol under pressure. n CONSTITUTION: One mole of a nitrile of the formula R 1 CN (R 1 is aryl, aralkyl, heterocyclic group, etc.) is reacted with 2W10mol of an aldehyde of the formula R 2 CHO (R 2 is H, alkyl, aryl, aralkyl, heterocyclic group, etc.) or 1mol of a ketone of the formula R 3 COR 4 (R 3 and R 4 are alkyl groups) in the presence of ammonia and 0.1W10mol of an alcohol under pressure to give the title substance of formula I or II. The amount of ammonia is 1.1W10mol per mole of the aldehyde or ketone, and the reaction pressure is 1,000W9,000kg/cm 2 . n COPYRIGHT: (C)1980,JPO&Japio
priorityDate 1978-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419550829
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410

Total number of triples: 18.