http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S62215567-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cff62ee19588f053fe1f229df4e6c756
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
filingDate 1986-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b73fe0c5d12671ab665f5d3c33efc43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_489de28ca332e562562b6dd33c5c31fa
publicationDate 1987-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S62215567-A
titleOfInvention Production of 2,2,6,6-tetramethyl-4-oxopiperidine
abstract PURPOSE: To produce the titled substance in high yield with few problems such as waste water treatment, by reacting acetone with 2,2,4,4,6-pentamethyl-2,3,4,5- tetrahydropyrimidine in the presence of a carbonic acid ester. n CONSTITUTION: The titled substance is produced by reacting 1mol of 2,2,4,4,6- pentamethyl-2,3,4,5-tetrahydropyrimidine with 3W15mol of acetone in the presence of a carbonic acid ester compound of formula XCOOR (X is Cl or Br; R is 1W3C alkyl) as a catalyst at ≥30°C for 1W20hr. The amount of the catalyst is 0.05W10wt% of the compound of formula. The reaction may be carried out in the copresence of a cocatalyst selected from bromine, iodine, sodium bromide, ammonium chloride and activated carbon at an amount of 0.1W5wt% of the compound of formula. n USE: Raw material for photostabilizer of polymers and intermediate for pharmaceuticals. n COPYRIGHT: (C)1987,JPO&Japio
priorityDate 1986-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 34.